The Turkish Journal of Pediatrics 2019 , Vol 61 , Num 4
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome
Semra Gürsoy 1 ,Yaşar Bekir Kutbay 2 ,Taha Reşid Özdemir 2 ,Filiz Hazan 3
1 Departments of Pediatric Genetics, Dr. Behcet Uz Children's Hospital, İzmir, Turkey
2 Department of Medical, Genetics, Tepecik Training and Research Hospital, İzmir, Turkey
3 Departments of Medical Genetics, Dr. Behcet Uz Children's Hospital; İzmir, Turkey
DOI : 10.24953/turkjped.2019.04.017 Keywords :
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