Heterozygous p.D61G Mutation in a Patient with Noonan Syndrome
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CİLT: 9 SAYI: 1
P: 4 - 5
Haziran 2017

Heterozygous p.D61G Mutation in a Patient with Noonan Syndrome

J Clin Res Pediatr Endocrinol 2017;9(1):4-5
1. Balikesir Atatürk State Hospital, Clinic Of Pediatric Endocrinology, Balikesir, Turkey
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