Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Speiser, P W

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [electronic resource] - The Journal of clinical investigation Aug 1992 - 584-95 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0021-9738

10.1172/JCI115897 doi


Adrenal Hyperplasia, Congenital--genetics
Alleles
Base Sequence
Chromosome Deletion
Gene Frequency
Humans
Molecular Sequence Data
Mutation
Oligodeoxyribonucleotides--chemistry
Oligonucleotide Probes
Pedigree
Phenotype
Steroid 21-Hydroxylase--genetics