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Studies of the C-21 and C-19 Steroids and HLA Genotyping in Siblings and Parents of Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Overview
Journal J Clin Endocrinol Metab
Publisher Oxford University Press
Specialty Endocrinology
Date 1980 Mar 1
PMID 6244326
Citations 5
Authors
F LORENZEN
S Pang
M New
M Pollack
S Oberfield
B DuPont
D Chow
B Schneider
L Levine
Affiliations
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17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.

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