The 17 alpha-hydroxylase deficiency found in genotypically female and male siblings, both phenotypically female
Jinrui Idengaku Zasshi
.
1977 Mar;21(4):247-56.
Authors
S Ito
,
M Yamaguchi
,
N Miyamoto
,
T Yanase
PMID:
559816
No abstract available
Publication types
Case Reports
MeSH terms
Adolescent
Adult
Amenorrhea / genetics
Disorders of Sex Development / genetics*
Female
Genotype
Humans
Phenotype
Sex Chromosomes*
Steroid Hydroxylases / deficiency*
Substances
Steroid Hydroxylases