Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency

被引：0
|
作者：
Ayberk Turkyilmaz
Ceren Alavanda
Esra Arslan Ates
Bilgen Bilge Geckinli
Hamza Polat
Mehmet Gokcu
Taner Karakaya
Alper Han Cebi
Mehmet Ali Soylemez
Ahmet İlter Guney
Pinar Ata
Ahmet Arman
机构：
[1] Karadeniz Technical University,Department of Medical Genetics, School of Medicine
[2] Marmara University,Department of Medical Genetics, School of Medicine
[3] Marmara University Pendik Training and Research Hospital,Department of Medical Genetics
[4] Isparta City Hospital,Department of Medical Genetics
来源：
Journal of Assisted Reproduction and Genetics | 2022年 / 39卷
关键词：
SNP array; Primary ovarian insufficiency; Whole-exome sequencing;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：695 / 710
页数：15
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