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Tüysüz

Beyhan Tüysüz

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 242-248)

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 74-79)

Muscular Type Lipodystrophy Diagnosed with Neonatal Findings: Berardinelli-Seip Congenital Lipodystrophy Type 4 and Comparison Between the Types

(J Clin Res Pediatr Endocrinol 2017; 9: 30-31)

Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 27-27)

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

(J Clin Res Pediatr Endocrinol 2017; 9: 21-21)

A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 19-19)
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