Showing 1 - 8 results of 8 for search 'İbrahim KESER', query time: 0.03s Refine Results
  1. 1
    Complement Factor H Y403H Polymorphism in the Turkish Population

    Complement Factor H Y403H Polymorphism in the Turkish Population by Yunus Arikan, Türker Bilgen, Ibrahim Keser

    Published 2010-01-01
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  2. 2
    First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population

    First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population by Ibrahim Keser, Alev Öztaş, Türker Bilgen, Duran Canatan

    Published 2015-12-01
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  3. 3
    The effect of HBB:c.*+96T>C (3’UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype

    The effect of HBB:c.*+96T>C (3’UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype by Türker Bilgen, Duran Canatan, Yunus Arıkan, Akif Yeşilipek, İbrahim Keser

    Published 2011-09-01
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  4. 4
    The effect of HBB: c.*+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype

    The effect of HBB: c.*+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype by Türker Bilgen, Duran Canatan, Yunus Arıkan, Akif Yeşilipek, İbrahim Keser

    Published 2011-08-01
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  5. 5
    First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population

    First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population by Vildan Çiftçi, Duran Canatan, Türker Bilgen, Gülsüm Yazıcı, Serpil Delibaş, İbrahim Keser

    Published 2016-02-01
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  6. 6
    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

    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 Ant... by Türker Bilgen, Özden Altıok Clark, Zeynep Öztürk, M. Akif Yeşilipek, İbrahim Keser

    Published 2016-05-01
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  7. 7
    Cytogenetic and Molecular Investigation in Children with Possible Fragile X Syndrome

    Cytogenetic and Molecular Investigation in Children with Possible Fragile X Syndrome by Onur Ozer, Osman Demirhan, Erdal Tunc, Huseyin Bagci, Dilara Karahan, Nilgun Tanriverdi, Bertan Yilmaz, Ali Irfan Guzel, Ibrahim Keser

    Published 2012-04-01
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  8. 8
    Frajil X Sendromu Olduklarından Şüphelenilen Çocuklarda Sitogenetik ve Moleküler Araştırmalar

    Frajil X Sendromu Olduklarından Şüphelenilen Çocuklarda Sitogenetik ve Moleküler Araştırmalar by Onur ÖZER, Osman DEMİRHAN, Erdal TUNC, Hüseyin BAĞCI, Dilara KARAHAN, Nilgün TANRİVERDİ, Bertan YILMAZ, Ali İrfan GÜZEL, İbrahim KESER

    Published 2012-06-01
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