AUTHOR INDEX

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Türkkahraman

Doğa Türkkahraman

Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene

(J Clin Res Pediatr Endocrinol 2012; 4: -)

CTLA-4 (+49A/G) Polymorphism and Type-1 
Diabetes in Turkish Children

(J Clin Res Pediatr Endocrinol 2013; 5: -)

Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children

(J Clin Res Pediatr Endocrinol 2014; 6: 209-215)

High-Dose Hook Effect in 17-Hydroxyprogesterone Assay in a Patient with 21-Hydroxylase Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 329-332)

Letter to the Editor regarding “Testotoxicosis: Report of Two Cases, One with a Novel Mutation in Luteinizing Hormone/Choriogonadotropin Receptor Gene”

(J Clin Res Pediatr Endocrinol 2015; 7: 355-355)

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

(J Clin Res Pediatr Endocrinol 2016; 8: 205-210)

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

(J Clin Res Pediatr Endocrinol 2017; 9: 80-84)
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