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Hiort

Olaf Hiort

Long-Term Follow-Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5 - Case Report

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 249-252)

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)
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