Prof.Dr. İBRAHİM KESER

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C.

Bilgen T., Canatan D., Delibas S., Keser I.

Hemoglobin , cilt.40, ss.280-2, 2016 (SCI-Expanded)

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya.

Bilgen T., Altıok Clark Ö., Öztürk Z., Yeşilipek M. A., Keser İ.

Turkish journal of haematology : official journal of Turkish Society of Haematology , cilt.33, ss.107-11, 2016 (SCI-Expanded)

First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population.

Canatan D., Bilgen T., Çiftçi V., Yazıcı G., Delibaş S., Keser İ.

Turkish journal of haematology : official journal of Turkish Society of Haematology , cilt.33, ss.71-2, 2016 (SCI-Expanded)

First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population.

Keser İ., Öztaş A., Bilgen T., Canatan D.

Turkish journal of haematology : official journal of Turkish Society of Haematology , cilt.32, ss.374-5, 2015 (SCI-Expanded)

Clinical evaluation of R202Q alteration of MEFV genes in Turkish children

ÇOMAK E., AKMAN S., KOYUN M., Dogan C. S., Gokceoglu A. U., Arikan Y., et al.

CLINICAL RHEUMATOLOGY , cilt.33, sa.12, ss.1765-1771, 2014 (SCI-Expanded)

The Spectrum Of Mefv Clinical Presentations: Evaluation Of Children With Vasculitis

ÇOMAK E., Dogan C. S., Gokcoglu A. U., KESER İ., KOYUN M., AKMAN S.

PEDIATRIC NEPHROLOGY , cilt.29, sa.9, ss.1803, 2014 (SCI-Expanded)

MEFV gene mutations in Turkish children with juvenile idiopathic arthritis

Comak E., Dogan C. S., AKMAN S., KOYUN M., Gokceoglu A. U., KESER İ.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.172, sa.8, ss.1061-1067, 2013 (SCI-Expanded)

PREVELANCE OF MEFV GENE MUTATIONS IN CHILDREN WITH CELIAC DISEASE

ÇOMAK E., CEYHAN DOĞAN S., Gokceoglu A. U., Keser I., Artan R., Yilmaz A., et al.

ANNALS OF THE RHEUMATIC DISEASES , cilt.72, ss.996, 2013 (SCI-Expanded)

MEDITERRANEAN FEVER GENE: EVALUATION OF CLINICAL PRESENTATIONS IN TURKISH CHILDREN

ÇOMAK E., CEYHAN DOĞAN S., Gokceoglu A. U., KESER İ., Artan R., Yilmaz A., et al.

ANNALS OF THE RHEUMATIC DISEASES , cilt.72, ss.729, 2013 (SCI-Expanded)

Two novel mutations in the 3 ' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia

BILGEN T., CLARK O. A., OZTURK Z., YESILIPEK M. A., KESER İ.

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY , cilt.35, sa.1, ss.26-30, 2013 (SCI-Expanded)

A patient with Down syndrome with a de novo derivative chromosome 21

Cetin Z., Yakut S., MIHÇI E., MANGUOĞLU A. E., Berker S., KESER İ., et al.

GENE , cilt.507, sa.2, ss.159-164, 2012 (SCI-Expanded)

Expressional Analyses of NM23-H1, KAI1 and MKK4 Metastasis-Related Genes in Metastatic Ovarian Carcinomas

BILGEN T., ERDOĞAN G., ŞİMŞEK T., GULKESEN H., Pestereli E., Karaveli S., et al.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.32, sa.4, ss.984-989, 2012 (SCI-Expanded)

c.428_451 dup(24bp) MUTATION OF THE ARX GENE DETECTED IN A TURKISH FAMILY

Arikan Y., Bilgen T., Koken R., TURAN S., MIHÇI E., KESER İ.

GENETIC COUNSELING , cilt.23, sa.3, ss.367-373, 2012 (SCI-Expanded)

The association between inherited thrombophilias and pregnancy-related hypertension recurrence

Mendilcioglu I., Bilgen T., Arikan Y., KESER İ., ŞİMŞEK M., Timuragaoglu A.

ARCHIVES OF GYNECOLOGY AND OBSTETRICS , cilt.284, sa.4, ss.837-841, 2011 (SCI-Expanded)

**The effect of HBB:c.*+96T > C (3 ' UTR+1570 T > C) on the mild beta-thalassemia intermedia phenotype**

Bilgen T., Canatan D., Ankan Y., Yesilipek A., KESER İ.

TURKISH JOURNAL OF HEMATOLOGY , cilt.28, sa.3, ss.219-222, 2011 (SCI-Expanded)

hMLH1 Gene is not Methylated in Osteosarcoma

BİLGEN T., KESER İ.

LABMEDICINE , cilt.42, sa.5, ss.280-282, 2011 (SCI-Expanded)

The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population

Bilgen T., Arikan Y., Canatan D., Yesilipek A., KESER İ.

BLOOD CELLS MOLECULES AND DISEASES , cilt.46, sa.3, ss.226-229, 2011 (SCI-Expanded)

Pure and Complete 12p Trisomy Due To a Maternal Centric Fission of Chromosome 12

Cetin Z., MIHÇI E., Yakut S., KESER İ., Karauzum S. B., Luleci G.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.155A, sa.2, ss.349-352, 2011 (SCI-Expanded)

PRENATAL DIAGNOSIS OF beta-THALASSEMIA AND OTHER HEMOGLOBINOPATHIES IN SOUTHWESTERN TURKEY

Mendilcioglu I., Yakut S., KESER İ., ŞİMŞEK M., YESILIPEK A., BAGCI G., et al.

HEMOGLOBIN , cilt.35, sa.1, ss.47-55, 2011 (SCI-Expanded)

PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCYGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE

DÜNDAR M., Uzak A., ERDOĞAN M., Saatci C., AKDENİZ Ş., LULECI G., et al.

GENETIC COUNSELING , cilt.22, sa.2, ss.199-205, 2011 (SCI-Expanded)

EVALUATION OF SELF-ESTEEM WITH INTERNALIZED STIGMATIZATION IN THE PATIENTS WITH MENTALLY ILLNESS

Keser I., Saygin N., Turkan S., Kulaksizoglu B., Buldukoglu K.

EUROPEAN PSYCHIATRY , cilt.26, 2011 (SCI-Expanded)

Screening of the HFE Gene Mutations in Turkish Patients with Cryptogenic Cirrhosis and Hemochromatosis

ÖZTÜRK S., DIKICI H., DİNÇER D., Luleci G., KESER İ.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.30, sa.6, ss.1891-1895, 2010 (SCI-Expanded)

Evaluation of congenital heart diseases and thyroid abnormalities in children with Down syndrome

MIHÇI E., Akcurin G., Eren E., Kardelen F., Akcurin S., KESER İ., et al.

ANATOLIAN JOURNAL OF CARDIOLOGY , cilt.10, sa.5, ss.440-445, 2010 (SCI-Expanded)

Familial Mediterranean Fever and Henoch - Schonlein Purpura: Similar Symptoms but Different Diagnosis

Dogan C. S., ÇOMAK E., Koyun M., Gokceoglu A. U., Keser I., AKMAN S.

PEDIATRIC NEPHROLOGY , cilt.25, sa.9, ss.1865, 2010 (SCI-Expanded)

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

USLU A., OGUS C., ÖZDEMİR T., BİLGEN T., TOSUN O., KESER İ.

BMB REPORTS , cilt.43, sa.8, ss.530-534, 2010 (SCI-Expanded)

Insertion/Deletion Polymorphism and Serum Activity of the Angiotensin-Converting Enzyme in Turkish Patients with Obstructive Sleep Apnea Syndrome

OGUS C., KET S., BİLGEN T., KESER İ., ÇİLLİ A., GOCMEN A. Y., et al.

BIOCHEMICAL GENETICS , cilt.48, sa.5-6, ss.516-523, 2010 (SCI-Expanded)

Abnormal hemoglobins associated with the beta-globin gene in Antalya province, Turkey

KESER İ., YEŞİLİPEK A., CANATAN D., LULECI G.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.40, sa.1, ss.127-131, 2010 (SCI-Expanded)

Neutrophil Oxidative Metabolism in Down Syndrome Patients With Congenital Heart Defects

AKINCI O., MIHÇI E., TACOY S., KARDELEN F., KESER İ., ASLAN M.

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS , cilt.51, sa.1, ss.57-63, 2010 (SCI-Expanded)

Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies

MIHÇI E., ÖZCAN M., BERKER-KARAUZUM S., KESER İ., TACOY S., HAPSOLAT S., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.5, ss.453-459, 2009 (SCI-Expanded)

DNA Gains and Losses of Chromosome in Laryngeal Squamous Cell Carcinoma Using Comparative Genomic Hybridization

KESER İ., Toraman A. D., ÖZBİLİM G., GÜNEY K., LÜLECİ G.

YONSEI MEDICAL JOURNAL , cilt.49, sa.6, ss.949-954, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

Relationship between SP1 polymorphism and osteoporosis in beta-thalassemia major patients

GUZELOGLU-KAYISLI O., CETIN Z., KESER İ., OZTURK Z., TUNCER T., CANATAN D., et al.

PEDIATRICS INTERNATIONAL , cilt.50, sa.4, ss.474-476, 2008 (SCI-Expanded)

Frequencies of four genetic polymorphisms in the CYP1A2 gene in Turkish population

BILGEN T., TOSUN Ö., LULECI G., KESER İ.

RUSSIAN JOURNAL OF GENETICS , cilt.44, sa.8, ss.989-992, 2008 (SCI-Expanded)

Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism

ŞİMŞEK M., Cetin Z., BİLGEN T., Taskin O., Luleci G., KESER İ.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , cilt.34, sa.1, ss.73-77, 2008 (SCI-Expanded)

Primary atypical teratoid/rhabdoid tumor of the clival region - Case report

Kazan S., Goksu E., Mihci E., Gokhan G., Keser I., Gurer I.

JOURNAL OF NEUROSURGERY , cilt.106, sa.4, ss.308-311, 2007 (SCI-Expanded)

Frequency of three hemochromatosis gene mutations in Antalya, Turkey

ÖZTÜRK S., LULECI G., KESER İ.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.10, sa.1, ss.25-28, 2007 (SCI-Expanded)

Prenatal diagnosis of β-thalassemia in the Antalya Province

KESER İ., Manguoğlu E., GÜZELOGLU KAYIŞLI Ö., KURT F., MENDILCIOGLU I., ŞİMŞEK M., et al.

Turkish Journal of Medical Sciences , cilt.35, sa.4, ss.251-253, 2005 (SCI-Expanded)

Two rare mutations in Turkey: IVSI.130(G-C) and IVSII.848(C-A)

Nal N., MANGUOGLU A. E., SARGIN C. F., KESER I., Kupesiz A., Yesilipek A., et al.

CLINICAL AND LABORATORY HAEMATOLOGY , cilt.27, sa.4, ss.274-277, 2005 (SCI-Expanded)

Combination of IVS2.849 A-G with IVS1.1 G-A: A mutation of beta-globin gene in a Turkish beta-thalessemia major patient

Manguoglu E., SARGIN C. F., Nal N., KESER İ., Kupesiz A., Yesilipek A., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.22, sa.4, ss.291-295, 2005 (SCI-Expanded)

The phenotypic effect of Hb G-Coushatta [beta 22 (B4) Glu-Ala] and association with IVS. II.1 (G-A) in a Turkish family

Sargin C., Nal N., Manguoglu A. E., Keser I., Mendilcioglu I., Yesilipek A., et al.

GENETIC COUNSELING , cilt.16, sa.3, ss.307-308, 2005 (SCI-Expanded)

Netherton syndrome associated with idiopathic congenital hemihypertrophy

Yerebakan O., Uguz A., Keser I., Luleci G., Ciftcioglu M. A., Basaran E., et al.

PEDIATRIC DERMATOLOGY , cilt.19, sa.4, ss.345-348, 2002 (SCI-Expanded)

Epidermodysplasia verruciformis associated with neurofibromatosis type 1: coincidental association or model for understanding the underlying mechanism of the disease?

Alpsoy E., Ciftcioglu M. A., Keser I., De Villiers E., Zouboulis C.

BRITISH JOURNAL OF DERMATOLOGY , cilt.146, sa.3, ss.503-507, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

Comparative genomic hybridization in ganglioneuroblastomas

TORAMAN A., Keser I., Luleci G., TUNALI N., GELEN T.

CANCER GENETICS AND CYTOGENETICS , cilt.132, sa.1, ss.36-40, 2002 (SCI-Expanded)

Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation T(18p;21Q) by fluorescence in situ hybridisation

Alkan M., Ramelli G., Hirsiger H., Keser I., Remonda L., Buhler E., et al.

GENETIC COUNSELING , cilt.13, sa.2, ss.151-156, 2002 (SCI-Expanded)

Sickle-beta-thalassemia and splenic calcification

SENOL U., LULECI E., Keser I., GUZELOGLU-KAYISH O., TORAMAN A., Luleci G., et al.

ABDOMINAL IMAGING , cilt.26, sa.5, ss.557, 2001 (SCI-Expanded)

beta-thalassemia major associated with Down syndrome

Keser I., Canatan D., GUZELOGLU-KAYISLI O., COSAN R., Luleci G.

ANNALES DE GENETIQUE , cilt.44, sa.2, ss.57-58, 2001 (SCI-Expanded)

Hb antalya [codons 3-5 (Leu-Thr-Pro -> Ser-Asp-Ser)]: A new unstable variant leading to chronic microcytic anemia and high Hb A(2)

Keser I., Kayisli O., Yesilipek A., OZES O. N., Luleci G.

HEMOGLOBIN , cilt.25, sa.4, ss.369-373, 2001 (SCI-Expanded)

Fragile (12)(q13) chromosome associated with mental retardation and bilateral congenital cataract

Keser I., Luleci G., Sisli S.

CYTOGENETICS AND CELL GENETICS , cilt.85, sa.1-2, ss.153, 1999 (SCI-Expanded)

Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as unbalanced translocation t(18p : 21q) by fluorescence in situ hybridization

Alkan M., Ramelli G., Hirsiger H., Keser I., Remonda L., Buhler E., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.6, ss.75, 1998 (SCI-Expanded)

Detection of gains and losses of genetic material in subtypes of rhabdomyosarcoma by comparative genomic hybridization using double step DOP-PCR

Alkan M., Keser I., Tunali N., Ortac R., Burckhardt E.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.6, ss.99, 1998 (SCI-Expanded)

Detection of Gains and losses of DNA sequences in five ganglioneuroblastoma by comparative genomic hybridization using double step DOP-PCR

Keser I., Burckhardt E., Ortac R., Tunali N., Caglar M., Alkan M.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.6, ss.99, 1998 (SCI-Expanded)

Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families

WANG Q., DESSEIGNE F., LASSET C., SAURIN J., NAVARRO C., YAGCI T., et al.

INTERNATIONAL JOURNAL OF CANCER , cilt.73, sa.6, ss.831-836, 1997 (SCI-Expanded) Sürdürülebilir Kalkınma

A new type familial translocation

Luleci G., Keser I., Baysal C.

CYTOGENETICS AND CELL GENETICS , cilt.77, sa.1-2, 1997 (SCI-Expanded)

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

BERNASCONI F., KARAGUZEL A., CELEP F., Keser I., Luleci G., DUTLY F., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.59, sa.5, ss.1114-1118, 1996 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Fetal hemoglobin altering effects of KLF1, BCL11A rs11886868 and XmnI-HBG2 on transfusion dependent beta thalassemia patients: Preeliminary study

ARIKAN Y., YOLCULAR B. O., KURTOĞLU E., KESER I.

Annals of Medical Research , cilt.30, sa.5, ss.598-603, 2023 (Hakemli Dergi)

FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center Tek Bir Merkezden FMR1 Gen Mutasyon Analizi ve CGG Tekrar Sayisi Daǧilimi

ARIKAN Y., Bilgen T., MIHÇI E., DUMAN Ö., Karaman T., KESER İ.

Gazi Medical Journal , cilt.34, sa.4, ss.369-374, 2022 (Scopus)

Investigation of alpha globin gene mutations by complementary methods in antalya

KESER İ., Mercan T., BILGEN T., KÜPESİZ O. A., ARIKAN Y., CANATAN D.

Eastern Journal of Medicine , cilt.26, sa.1, ss.117-122, 2021 (Scopus)

Molecular analysis of fragile X syndrome in Antalya Province

BİLGEN T., KESER İ., MIHÇI E., HASPOLAT Ş., TAÇOY Ş., LÜLECİ G.

INDIAN JOURNAL OF MEDICAL SCIENCES , cilt.59, ss.150-155, 2015 (Scopus)

Beta-Talasemi Taşıyıcılarında Beta-Globin Gen Mutasyon Tipi ve Hematolojik Fenotip Arasındaki İlişki

Öney S., Öztürk Z., KÜPESİZ O. A., Keser İ., Yeşilipek A.

Türk-Çocuk Hematoloji Dergisi , cilt.2, sa.4, ss.23-28, 2008 (Hakemli Dergi)

Prenatal Diagnosis of B-Thalassemia in the Antalya Province

KESER İ., MANGUOĞLU E., Kayisli O., Kurt F., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.35, ss.251-253, 2005 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Induction of fetal hemoglobin by modulation of epigenetic and genetic factors in beta thalassemia major patients

Keser I., Arikan Y., Kupesiz A., Bilgen T., Kurtoglu E.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.743-744

Malign Epitelyal Over Tümörlerinin Agresivitesinde AMP/GPI, AMFR, CTGF, RAB25, RASSF2A Genlerinin Öneminin Belirlenmesi

ÖZCAN M., KESER İ., ERDOĞAN G., PEŞTERELİ H. E.

27. Ulusal Patoloji Kongresi, Antalya, Türkiye, 15 - 18 Kasım 2017, ss.100

Antalya ve Çevresinde Alfa Globin Gen Mutasayonlarının Araştırılması

ARIKAN Y., BİLGEN T., KARAMAN T., CANATAN D., KESER İ.

Tıbbi Biyoloji Ve Genetik Kongresi, Muğla, Türkiye, 26 - 30 Ekim 2015, ss.346

Antalya ve Çevresinde Alfa Globin Gen Mutasyonlarının Araştırılması

ARIKAN Y., BİLGEN T., KARAMAN T., CANATAN D., KESER İ.

14.ULUSAL TIBBİ BİYOLOJİ ve GENETİK KONGRESİ, Muğla, Türkiye, 26 - 30 Ekim 2015, ss.346

CLINICAL EVALUATION OF R202Q ALTERATION OF MEFV GENES IN TURKISH CHILDREN: IS R202Q A BENIGN POLYMORPHISM OR A DISEASE-CAUSING MUTATION?

ÇOMAK E., AKMAN S., Dogan C. S., Gokceoglu A. U., Arikan Y., KESER İ.

15th Annual European Congress of Rheumatology (EULAR), Paris, Fransa, 11 - 14 Haziran 2014, cilt.73, ss.580

Evaluation of R202Q alteration of Pyrin Protein onto Familial Mediterrenan Fever (FMF) in Antalya Province

ARIKAN Y., BILGEN T., ÇOMAK E., AKMAN S., ALTIOK CLARK Ö., ARTAN R., et al.

The EMBO Meeting 2013, Amsterdam, Amsterdam, Hollanda, 21 - 24 Eylül 2013

Evaluation of R202Q alteration of Pyrin Protein onto Familial Mediterrenan Fever (FMF) in Antalya Province

ARIKAN Y., BILGEN T., ÇOMAK E., AKMAN S., ALTIOK CLARK Ö., ARTAN R., et al.

The EMBO Meeting 2013, Amsterdam, Amsterdam, Hollanda, 21 - 24 Eylül 2013, ss.78

Evaluation of R202Q alteration of Pyrin Protein onto Familial Mediterrenan Fever (FMF) in Antalya Province

ARIKAN Y., BILGEN T., ÇOMAK E., AKMAN S., ALTIOK CLARK Ö., ARTAN R., et al.

The EMBO Meeting 2013, Amsterdam, Amsterdam, Hollanda, 21 - 24 Eylül 2013

Molecular characterization of deletional forms of beta-thalassemia in Antalya, Turkey

KESER İ., BİLGEN T., ARIKAN Y., CANATAN D., YESİLİPEK A., CORNELIS H.

EUROPEAN HUMAN GENETISC CONFERENCE 2013, Paris, Fransa, 8 - 11 Haziran 2013, ss.563-564

ANTALYA'DA BETA GLOBİN GENİNDE GÖRÜLEN NADİR MUTASYONLAR

ARIKAN Y., BİLGEN T., YESİLİPEK A., CANATAN D., KESER İ.

6.ULUSLAR ARASI TALASEMİ KONGRESİ VE YAZ OKULU, Antalya, Türkiye, 18 - 23 Nisan 2013, ss.262

Prenatal Screening of Beta Thalassemia in Antalya, Turkey

BİLGEN T., ALTIOK CLARK Ö., ARIKAN Y., MENDİLCİOĞLU İ. İ., SAKINCI M., ŞİMŞEK M., et al.

6.ULUSLAR ARASI TALASEMİ KONGRESİ VE YAZ OKULU, Antalya, Türkiye, 18 - 23 Nisan 2013, ss.264

Twelve different abnormal hemoglobins in Antalya province, Turkey

KESER İ., BİLGEN T., ARIKAN Y., YESİLİPEK A., CANATAN D.

6.ULUSLAR ARASI TALASEMİ KONGRESİ VE YAZ OKULU, Antalya, Türkiye, 18 - 23 Nisan 2013, ss.266

Gap PCR Screening for Common Deletional Mutation of the Beta Globin Gene in the Antalya Province of Turkey

BİLGEN T., ALTIOK CLARK Ö., ARIKAN Y., CANATAN D., YESİLİPEK A., KESER İ.

6.ULUSLAR ARASI TALASEMİ KONGRESİ VE YAZ OKULU, Antalya, Türkiye, 18 - 23 Nisan 2013, ss.264

HbG Coushatta [Beta22(B4)Glu-Ala] ve Cod 2 C>T SNP arasındaki ilişki

ARIKAN Y., BİLGEN T., YESİLİPEK A., CANATAN D., KESER İ.

6.ULUSLAR ARASI TALASEMİ KONGRESİ VE YAZ OKULU, Antalya, Türkiye, 18 - 23 Nisan 2013, ss.263

**HBB:c.*+47 C>G: Beta-globin Geninin Yeni Bir Sessiz Mutasyonu**

Bilgen T., Albayrak C., Altıok Clark Ö., Albayrak D., Keser İ.

10. Ulusal Tıbbi Genetik Kongresi, Bursa, Türkiye, 19 - 23 Aralık 2012, ss.114

Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2011, ss.158-159

Antalya'da beta globin geninde delesyonel tip mutasyonların tanımlanması

KESER İ., BİLGEN T., ARIKAN Y., CANATAN D., YEŞİLİPEK A., CORNELIS L H.

12.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2011, ss.172

Down sendromu olgusunda gözlenen de novo Rekombinant Kromozom 21

ÇETİN Z., YAKUT S., MIHÇI E., MANGUOĞLU A. E., BERKER-KARAÜZÜM S., KESER İ., et al.

XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2011

Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2011, ss.158-159

Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Türkiye, 27 - 30 Ekim 2011, ss.158-159

A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Kanada, 11 - 15 Ekim 2011, ss.273

A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Kanada, 11 - 15 Ekim 2011, ss.273

A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Kanada, 11 - 15 Ekim 2011, ss.273

Two Rare Mutations: IVS-I (-3) (C>T) and Codon 69 (G>A) in Antalya Population

KESER İ., BİLGEN T., ARIKAN Y., YEŞİLİPEK A., CANATAN D.

12th International Conference on Thalassemia and Other Haemoglobinopathies, 14th TIF Conference for Patients and Parents, ANTALYA, Antalya, Türkiye, 4 - 07 Eylül 2011, ss.85

Abnormal Hemoglobins Detected in Antalya Population, Turkey

KESER İ., BARGİC G., BİLGEN T., ARIKAN Y., YESİLİPEK A., CANATAN D.

12th International Conference on Thalassemia and Other Haemoglobinopathies, 14th TIF Conference for Patients and Parents, Antalya, Türkiye, 4 - 07 Eylül 2011, ss.105

The Association Between the Intragenic SNP Haplotypes and Mutations of Beta Globin Gene in Turkey Population

BİLGEN T., ARIKAN Y., CANATAN D., YESİLİPEK A., KESER İ.

12th International Conference on Thalassemia and Other Haemoglobinopathies, 14th TIF Conference for Patients and Parents, Antalya, Türkiye, 4 - 07 Eylül 2011, ss.134

Detection of the Turkish Inversion-Deletion (Delta Beta) (0) Thalassemia in a Family Seeking Prenatal Diagnosis and Prevention

BİLGEN T., PHYLIPSEN M., ARIKAN Y., MENDİLCİOĞLU İ. İ., YEŞİLİPEK M. A., HARTEVELD C. L., et al.

12th International Conference on Thalassemia and Other Haemoglobinopathies, 14th TIF Conference for Patients and Parents, Antalya, Türkiye, 4 - 07 Eylül 2011, ss.84

Two cases with rare chromosomal abnormality of chromosome 12p presenting Pallister-Killian syndrome phenotype

YAKUT S., LÜLECİ G., MIHÇI E., ÇETİN Z., KESER İ., BERKER-KARAÜZÜM S.

9 th National Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.21

A RARE AND NEW SPLICE SITE MUTATIONLEADING BETA-THALASSEMIA MAJOR:CODON 29 (C > T)

KESER İ., BILGEN T., ARIKAN Y., OZTURK Z., KURT P., YESİLİPEK A.

9th National Medical Congress, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.83

Two Cases with Rare Chromosomal Abnormality of Chromosome 12p Presenting Pallister-Killian Syndrome Phenotype.

YAKUT S., Lüleci G., MIHÇI E., Cetin Z., KESER İ., BERKER S.

IX. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.21

Co-inheritance of Beta-Thalassemia and Fragile-X syndrome in a Turkish family

BİLGEN T., ARIKAN Y., MIHÇI E., DUMAN Ö., YEŞİLİPEK A., HASPOLAT Ş., et al.

9 th National Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.48

Molecular diagnosis of Fragile X syndrome and distribution of CGG repeats number in 5-UTR of FMR1 gene in Antalya province

ARIKAN Y., BİLGEN T., MIHÇI E., DUMAN Ö., HASPOLAT Ş., KESER İ.

9 th National Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Türkiye, 1 - 05 Aralık 2010, ss.97

Co-Inheritance of beta-thalassemia and fragile X syndrome in a Turkish family

KESER İ., BİLGEN T., ARIKAN Y., MIHÇI E., DUMAN Ö., YEŞİLİPEK A., et al.

ASHG-2010, Washington, Amerika Birleşik Devletleri, 2 - 06 Kasım 2010, ss.2362

Two cases with rare chromosomal abnormality of chromosome 12p presenting Pallister-Killian syndrome phenotype.

Lüleci G., MIHÇI E., Cetin Z., YAKUT S., KESER İ., BERKER S.

The American Society of Human Genetics Annual Meeting, Washington, Amerika Birleşik Devletleri, 2 - 06 Ekim 2010

Two cases with rare chromosomal abnormality of chromosome 12p presenting Pallister-Killian syndrome phenotype.

Lüleci G., MIHÇI E., Cetin Z., YAKUT S., KESER İ., BERKER S.

The American Society of Human Genetics Annual Meeting, Washington, Amerika Birleşik Devletleri, 2 - 06 Ekim 2010, ss.382

Complement Factor H Y402H Polymorphism in Turkish Population

ARIKAN Y., BILGEN T., KESER İ.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International participation, İstanbul, Türkiye, 1 - 05 Ekim 2010, ss.52

The Relationship Between the 3-UTR +1570 (T>C) Mutation in the Beta Globin Gene and Mild Beta-Thalassemia Intermedia

KESER İ., BILGEN T., ARIKAN Y., YESİLİPEK A., CANATAN D.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International participation, İstanbul, Türkiye, 1 - 05 Ekim 2010, ss.125

Molecular Diagnosis of Fragile X Syndrome and distribtion ofCGG repeats number in 5’UTR of FMR1 Gene in Antalya Province

ARIKAN Y., BILGEN T., MIHÇI E., DUMAN Ö., HASPOLAT Ş., KESER İ.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International participation, İstanbul, Türkiye, 1 - 05 Ekim 2010, ss.97

Co-Inheritance of Beta Thalassemia and Fragile –X Syndrome in Turkish Family

BİLGEN T., ARIKAN Y., MIHÇI E., DUMAN Ö., YESİLİPEK A., HASPOLAT Ş., et al.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International participation, İstanbul, Türkiye, 1 - 05 Ekim 2010, ss.48

Familial Mediterranean Fever and Henoch–Schönlein Purpura: Similar Symptoms but Different Diagnosis

DOĞAN Ç. S., ÇOMAK E., KOYUN M., USLU-GOKCEOGLU A., KESER İ., AKMAN S.

15th Congress of the International Pediatric Nephrology Association, New York, Amerika Birleşik Devletleri, 6 - 09 Eylül 2010, ss.1865

Results of prenatal cytogenetic screening at the prenatal laboratory of the Akdeniz University 1993-2009.

YAKUT S., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., Çalışkan M., BERKER S., KESER İ., et al.

Prenatal Diagnosis and Therapy, Amsterdam, Hollanda, 11 - 14 Temmuz 2010, ss.94

Kalıtsal Hastaliklar Ve Ötekileştirme

KESER İ., Keser İ., Saygın N., Ergün G.

17. Ulusal Sosyal Psikiyatri Kongresi, İstanbul, Türkiye, 1 - 04 Haziran 2010

The association between inherited thrombophilias and pregnancy-related hypertension recurrence

MENDİLCİOĞLU İ. İ., Bilgen T., Arikan Y., KESER İ., ŞİMŞEK M.

30th Annual Meeting of the Society-for-Maternal-Fetal-Medicine, Illinois, Amerika Birleşik Devletleri, 1 - 06 Şubat 2010, cilt.201

Periyodik Ateş Sendromlarında TNFRSF1A Gen Mutasyonlarının Rolü

BİNGÖL BOZ A., Akdeniz S., Dayar E., Çelmeli F., KESER İ., Lüleci G., et al.

XVII. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 3 - 07 Kasım 2009, ss.54

Homozygous promotor mutation [-30/-30] of beta-globin gene caused by maternal uniparental isodisomy of chromosome 11 in a fetus

KESER İ., BILGEN T., ARIKAN Y., MENDİLCİOĞLU İ. İ., YEŞİLİPEK A., LÜLECİ G.

American Society of Human Genetics, 59th Annual Meeting, 20 - 24 Ekim 2009, ss.152

Rare chromosomal abnormalities and the results of prenatal cytogenetic Diagnosis.

YAKUT S., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., BERKER S., KESER İ., Luleci G.

Mediterranean Medical Genetics Meeting, Ankara, Türkiye, 28 Haziran - 01 Temmuz 2009, ss.58

Craniofacial morphometric measurements in turkish children with B-thalassemia major

YILDIRIM F. B., ÖZSOY U., DEMİREL B. M., Öztürk Z., arıcan Y., SARIKCIOĞLU L., et al.

Ninth Congress of European Association of Clinical Anatomy, Prag, Çek Cumhuriyeti, 5 - 08 Eylül 2007, ss.497

"Craniofacial morphometric measurements in turkish children with B-thalassemia major

YILDIRIM F. B., OSYOY U., ÖZTÜRK Z., DEMİREL M., ARICAN R., KESER İ., et al.

Ninth Congress of European Association of Clinical Anatomy. Surg Radiol Anat, 29(6):497, Prague/Czechoslovakia. 5-8 September ( 2007)., Prag, Çek Cumhuriyeti, 5 - 08 Eylül 2007, cilt.29, sa.6, ss.497

Craniofacial morphometric measurements in Turkish children with beta thalassemia major

YILDIRIM F. B., ÖZSOY U., DEMİREL B. M., Arıcan R. Y., SARIKCIOĞLU L., Öztürk Z., et al.

Uluslararası katılımlı XI. Ulusal Anatomi Kongresi, Denizli, Türkiye, 26 - 29 Ekim 2007, cilt.1

Bone mineral density hormonal and biochemical measurements in Turkish children with beta thalassemia major

YILDIRIM F. B., ÖZSOY U., DEMİREL B. M., Arıcan R. Y., SARIKCIOĞLU L., Öztürk Z., et al.

Uluslar arası katılımlı XI. Ulusal Anatomi Kongresi, Denizli, Türkiye, 26 - 29 Ekim 2007, cilt.1

De novo duplication dup(4)(q27q31.3) in a patient with charge association

ÇETİN Z., MIHÇI E., BERKER-KARAÜZÜM S., KESER İ., TAÇOY Ş., LÜLECİ G.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.71

Combination of Hb Knossos [Cod 27 (G-T)]and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major

KESER İ., MANGUOĞLU ., Kayisli O., Yesilipek A., Luleci G.

European Human Genetics Conference 2007, Nice, Fransa, 16 - 19 Haziran 2007, ss.18-19

Choanal atresia and mega-cisterna magna in a case with interstitial deletion of 13q22-q32

Keser I., ÇETİN Z., Mihci E., TAÇOY S., LÜLECİ G.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.104

De novo duplication dup(4)(q27q31.3) in a patient with charge association

Cetin Z., Mihci E., Berker-Karauzum S., Keser I., Tacoy S., Luleci G.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.71

Oxidative metabolism in down syndrome patients with congenital heart defects

Akinci O., Michi E., Tacoy S., KARDELEN F., KESER İ., AYDIN ASLAN M.

14th Annual Meeting of the Society-for-Free-Radical-Biology-and-Medicine, Washington, Kiribati, 14 - 18 Kasım 2007, cilt.43

Frajil X sendromlu olguların klinik bulgularının değerlendirilmesi

MIHÇI E., TAÇOY Ş., BİLGEN T., KESER İ., DUMAN Ö., LÜLECİ G.

50. Milli Pediatri Kongresi, Antalya, Türkiye, 8 - 12 Kasım 2006, ss.157

The Spectrum of Abnormal Hemoglobins in Antalya Province, Mediterranean Region of Turkey

KESER İ., MANGUOĞLU AYDEMİR A. E., Kayisli O., ŞANLIOĞLU A. D., ŞİMŞEK M., MENDİLCİOĞLU İ. İ.

31st FEBS Congress, İstanbul, Türkiye, 24 - 29 Haziran 2006, ss.354

The effects of the OPRM1 gene polymorphisims on pain control in Turkish patients

ÖZCAN M., MANGUOĞLU ., KESER İ., AKBAŞ M., KARSLI B., Luleci G.

31st FEBS Congress, İstanbul, Türkiye, 24 - 29 Haziran 2006, ss.261

The effects of the OPRM1 gene polymorphisims on pain control in Turkish patients

ÖZCAN M., MANGUOĞLU ., KESER İ., AKBAŞ M., KARSLI B., Luleci G.

31st FEBS Congress, İstanbul, Türkiye, 24 - 29 Haziran 2006, ss.261

The Effects Of The Oprm1 Gene Polymorphisims On Pain Control In Turkish Patients

ÖZCAN M., MANGUOĞLU A. E., KESER İ., AKBAŞ M., KARSLI B.

31st FEBS Congress, İstanbul, Türkiye, 24 - 29 Haziran 2006, ss.100

The Spectrum of Abnormal Hemoglobins in Antalya Province, Mediterranean Region of Turkey

KESER İ., MANGUOĞLU AYDEMİR A. E., Kayisli O., ŞANLIOĞLU A. D., ŞİMŞEK M., MENDİLCİOĞLU İ. İ.

31st FEBS Congress, İstanbul, Türkiye, 24 - 29 Haziran 2006, ss.354

The effects of the OPRM1 gene polymorphisms on pain control in Turkish patients.

Caliskan M. O., Manguoglu E., Keser I., Akbas M., KARSLI B., Akbas H., et al.

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.261

The spectrum of abnormal hemoglobins in Antalya province, Mediterranean region of Turkey

Keser I., Aydemir E., Kayisli O., Sanlioglu A., Simsek M., MENDİLCİOĞLU İ. İ., et al.

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.354

Cockayne sendromu ve kolonik adenokarsinom birlikteliği bulunan nadir bir olgu

TAÇOY Ş., MIHÇI E., BONEVAL C., KESER İ., ELPEK Ö., YILMAZ A., et al.

42. Türk Pediatri Kongresi, Antalya, Türkiye, 15 - 20 Mayıs 2006, ss.15-20

Antalya'da Beta-Talasemi ve Orak Hücre Anemide Yapılan Moleküler Genetik Çalışmalar

KESER İ., MANGUOĞLU A. E., ŞANLIOĞLU A. D., Kayisli O., Sargin F., Nal N., et al.

Huisman Memorial Symposium II, Adana, Türkiye, 7 - 08 Mayıs 2006, ss.14-15

Ailesel intrakraniyal anevrizmalar; 7 olgu

GÖKSU E. T., Bilgen T., KESER İ., AKYÜZ M., TUNCER M. R.

TND 19. Bilimsel Kongresi, Antalya, Türkiye, 27 - 31 Mayıs 2005, ss.123

Ailesel intrakraniyal anevrizmalar; 7 olgu

GÖKSU E. T., Bilgen T., KESER İ., AKYÜZ M., TUNCER M. R.

TND 19. Bilimsel Kongresi, Antalya, Türkiye, 27 - 31 Mayıs 2005, ss.123

Prenatal diagnosis of duplication of chromosome 14q resulting from crossingover within a paternal pericentric inversion

BAĞCI G., ÖZCAN M., ÖZTÜRK S., KESER İ., MENDİLCİOĞLU İ. İ., LÜLECİ G.

The european society of human genetics conference, Prag, Çek Cumhuriyeti, 7 - 10 Mayıs 2005, ss.172

Screening of the HFE gene mutations in patients with cryptogenic cirrhosis by PCR-RFLP technique

ÖZTÜRK S., KESER İ., Dikici H., DİNÇER D., Lüleci G.

The european society of human genetics conference, Prag, Çek Cumhuriyeti, 7 - 10 Mayıs 2005, ss.232

Prenatal diagnosis of duplication of chromosome 14q resulting from crossingover within a paternal pericentric inversion

BAĞCI G., ÖZCAN M., ÖZTÜRK S., KESER İ., MENDİLCİOĞLU İ. İ., LÜLECİ G.

The european society of human genetics conference, Prag, Çek Cumhuriyeti, 7 - 10 Mayıs 2005, ss.172

Prenatal diagnosis of duplication of chromosome 14q resulting from crossingover within a paternal pericentric inversion

BAĞCI G., ÖZCAN M., ÖZTÜRK S., KESER İ., MENDİLCİOĞLU İ. İ., LÜLECİ G.

The european society of human genetics conference, Prag, Çek Cumhuriyeti, 7 - 10 Mayıs 2005, ss.172

Prenatal diagnosis of duplication of chromosome 14q resulting from crossingover within a paternal pericentric inversion

BAĞCI G., ÖZCAN M., ÖZTÜRK S., KESER İ., MENDİLCİOĞLU İ. İ., LÜLECİ G.

The european society of human genetics conference, Prag, Çek Cumhuriyeti, 7 - 10 Mayıs 2005, ss.172

The effect of CYP3A5 and P-glycoprotein (MDR-1) polymorphisms on tacrolimus dose requirement in renal transplant patients

AKBAŞ S. H., Keser I., Bilgen T., Tuncer M., Gultekin M., Luleci G.

European Congress of Clinical Biochemistry and Laboratory Medicine (EUROMEDLAB 2005), Glasgow, Birleşik Krallık, 8 - 12 Mayıs 2005, cilt.355

Prenatal diagnosis of duplication of chromosome 14q resulting from crossingover within a paternal pericentric inversion.

Bağcı G., ÖZCAN M., KESER İ., ÖZTÜRK S., MENDİLCİOĞLU İ. İ.

Fetal Tıp; Prenatal Tanı, Antalya, Türkiye, 30 Nisan - 02 Mayıs 2005, ss.100

Hb Knossos [Cod27 (G-T)] in a Turkish Patient with Beta-Thalassemia Major

Öztürk Z., MANGUOĞLU ., Kayisli O., KESER İ., KÜPESİZ O. A., Lüleci G.

Advances in Molecular Medicine, İstanbul, Türkiye, 16 - 19 Nisan 2005, ss.394-395

Compound heterozygosity for E230K and M694V variants of MEFV gene in a FMF patient. p.020, Istanbul, Adv Mol Med, Vol.1, Suppl.1, P020, pp:392

Guzeloglu-Kayisli O., KURT F., KESER İ., YAZISIZ V., LÜLECİ G.

1st Congress of Molecular Medicine,, İstanbul, Türkiye, 16 - 19 Nisan 2005, cilt.1, ss.392

A New allelic variant K695M in the MEFV gene in a Turkish family suffering from FMF

KESER İ., MANGUOĞLU E., Özgüven e., Lüleci G.

European Human Genetics Conference 2004, Münih, Almanya, 12 - 15 Haziran 2004, ss.221

Ailesel Akdeniz Ateşi Olan Bir Ailede MEFV Geninde Tanımlanan Yeni Bir Allelik Varyant: K695M

KESER İ., MANGUOĞLU E., Özgüven e., Lüleci G.

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Türkiye, 21 - 24 Nisan 2004, ss.90

Türkiye'de tanımlanan iki nadir mutasyon: IVS1.130 G-C ve IVS2.848 C-A

Nal N., MANGUOĞLU A. E., Sargın C., KESER İ., KÜPESİZ O. A., Yesilipek A., et al.

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Türkiye, 21 - 24 Nisan 2004, ss.107-108

Genetik Stigmatizasyon

KESER İ., Kukulu K., Ergün G., Keser İ.

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Türkiye, 1 - 04 Nisan 2004, ss.110

A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis

Nal N., Sargin F., MANGUOĞLU E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.

European Human Genetics Conference 2003, Birmingham, Birleşik Krallık, 3 - 06 Mayıs 2003, ss.241

Beta Talasemi Taşıyıcılarında Beta Globulin Gen Mutasyonları ve Hematolojik Parametreler

Öney S., Keser İ., KÜPESİZ O. A., Yeşilipek M. A., Lüleci G.

II. Ulusal Hemoglobinopati Kongresi, Adana, Türkiye, 30 Ekim - 01 Kasım 2002, ss.79

Antalya'da B-Talasemi ve Orak Hücre Anemide Yapılan Moleküler Genetik Çalışmalar

Keser İ., Güzeloğlu Ö., Toraman A., Manguoğlu A., Lüleci G., Yeşilipek M. A., et al.

II. Ulusal Hemoglobinopati Kongresi, Adana, Türkiye, 30 Ekim - 01 Kasım 2002, ss.79

Beta Talasemide Nadir Bir Mutasyon ve Prenatal Tanısı Kodon 22 (A-C)

Sargın C., Nal N., MANGUOĞLU AYDEMİR A. E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Türkiye, 9 - 12 Ekim 2002, ss.193

Antalya'da Beta-Talasemi ve Orak Hücreli Anemide Yapılan Moleküler Genetik Çalışmalar

KESER İ., ŞANLIOĞLU A. D., Kayisli O., MANGUOĞLU A. E., Sargin F., Nal N., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Türkiye, 9 - 12 Ekim 2002, ss.70

Frajil X sendromunda nonradyoaktif moleküller genetik çalışmalar

BİLGEN T., KESER İ., TAÇOY Ş., MIHÇI E., HASPOLAT Ş., LÜLECİ G.

5. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Türkiye, 9 - 12 Ekim 2002, ss.191

Beta Talasemide Nadir Bir Mutasyon ve Prenatal Tanısı Kodon 22 (A-C)

Sargın C., Nal N., MANGUOĞLU AYDEMİR A. E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Türkiye, 9 - 12 Ekim 2002, ss.193

Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province.

BILGEN T., KESER İ., Mihci E., Tacoy S., HASPOLAT S., Luleci G.

British Human Genetics Conference 2002, York, Sierra Leone, 23 - 25 Eylül 2002, cilt.39

Identification of deaoxyribonucleic acid copy number changes in larynx carcinoma by comparative genomic hybridization

Lüleci G., KESER İ., ŞANLIOĞLU A. D., ÖZBİLİM G., GÜNEY K.

European Society of Human Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.109

Identification of deoxyribonucleic acid copy number changes in larynx carcinoma by comparative genomic hybridization

Lüleci G., KESER İ., TORAMAN A., ÖZBİLİM G., GÜNEY K.

European Human Genetics Conference, Strazburg, Fransa, 25 - 29 Mayıs 2002, cilt.10 Supp, ss.109

Identification of deaoxyribonucleic acid copy number changes in larynx carcinoma by comparative genomic hybridization

Lüleci G., KESER İ., ŞANLIOĞLU A. D., ÖZBİLİM G., GÜNEY K.

European Society of Human Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.109

A Rare Mutation of Beta-Globin Gene (IVS 2-849 A>G) at Exon2-Intron2 Splice Site in a Turkish Patient with Beta-Thalassemia Major

Sargın C., MANGUOĞLU E., Nal N., KESER İ., Yesilipek A., Lüleci G.

European Human Genetics Conference 2002, Strazburg, Fransa, 25 - 29 Mayıs 2002, ss.204

sp1 gene polymorphism in patients with Beta-Thalassemia major

Toraman A., Kayisli O., Keser I., Cosan R., Canatan D., Luleci G.

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.203

Identification of two novel beta Thalassemia mutations and a novel compound heterozygosity in Antalya population: Hb Antalya, Cod 3 (+T)/IVS1.110, Hb Tyne/Hb S

Kayisli O., Toraman A., Keser I., Yesilipek A., Canatan D., Luleci G.

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.204

A rare mutation of beta-globin gene (IVS 2-849 A -> G) at Exon 2-intron 2 splice site in a Turkish patient with beta-thalassaemia major

Sargin C., Aydemir A., Nal N., Keser I., Yesilipek A., Luleci G.

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.204

Identification of deoxyribonucleic acid copy number changes in larynx carcinoma by comparative genomic hybridization

Luleci G., Keser I., Toraman A., Ozbilim G., Guney K.

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.109