Open AccessPhenotype-Genotype Correlation in 56 Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Author(s) -
Catherine DeneuxTharaux
Publication year - 2001
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.86.1.207
Subject(s) - genotype , allele , congenital adrenal hyperplasia , genetics , phenotype , loss of heterozygosity , locus (genetics) , 21 hydroxylase , biology , compound heterozygosity , genotype phenotype distinction , mutation , heterozygote advantage , gene , basal (medicine) , medicine , endocrinology , insulin
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