TY  - GEN
AU  - Speiser,P W
AU  - Laforgia,N
AU  - Kato,K
AU  - Pareira,J
AU  - Khan,R
AU  - Yang,S Y
AU  - Whorwood,C
AU  - White,P C
AU  - Elias,S
AU  - Schriock,E
TI  - First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
SN  - 0021-972X
PY  - 1990///0510
KW  - Adrenal Hyperplasia, Congenital
KW  - diagnosis
KW  - Adult
KW  - Amniocentesis
KW  - Chorionic Villi
KW  - ultrastructure
KW  - Dexamethasone
KW  - therapeutic use
KW  - Female
KW  - Fetal Diseases
KW  - Genetic Counseling
KW  - Humans
KW  - Karyotyping
KW  - Pedigree
KW  - Polymorphism, Restriction Fragment Length
KW  - Pregnancy
KW  - Pregnancy Trimester, First
KW  - Prenatal Diagnosis
KW  - Steroid Hydroxylases
KW  - deficiency
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1210/jcem-70-4-838
ER  -