Hasil Pencarian - Burhan BALTA

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  1. 1
    The Role of Chromosome Analysis in Patients with Recurrent Pregnancy Loss

    The Role of Chromosome Analysis in Patients with Recurrent Pregnancy Loss oleh Burhan BALTA, Murat ERDOĞAN, Aslıhan KİRAZ, Zeki YILMAZ

    Diterbitkan 2021-04-01
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  2. 2
    A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

    A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G oleh Burhan Balta, Murat Erdoğan, Aslıhan Kiraz, Serdal Korkmaz, Alperen Ağadayı

    Diterbitkan 2019-02-01
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  3. 3
    A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome

    A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome oleh Gozde Ozcan, Burhan Balta, Ahmet Ercan Sekerci, Osman A Etoz, Claudia Martinuzzi, Ozlem Kara, Lorenza Pastorino, Fatma Kocoglu, Omer Ulker, Murat Erdogan

    Diterbitkan 2016-01-01
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  4. 4
    The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

    The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey oleh Murat Erdoğan, Mehmet Köse, Sevgi Pekcan, Melih Hangül, Burhan Balta, Aslıhan Kiraz, Gizem Akıncı Gönen, Ayşe Gül Zamani, Mahmut Selam Yıldırım, Tuğba Ramaslı Gürsoy, Fatih Ezgu, Tuğba Şişmanlar Eyüpoğlu, Ayse Tana Aslan

    Diterbitkan 2021-11-01
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