Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: Evidence for further genetic heterogeneity in this syndrome

Proceedings of the National Academy of Sciences of the United States of America

Volumn 85, Issue 21, 1988, Pages 8151-8155

  Brown, T R ^a   Lubahn, D B ^a   Wilson, E M ^a   Joseph, D R ^a   French, F S ^a   Migeon, C J ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; COMPLEMENTARY DNA;

CASE REPORT; GENE DELETION; GENETIC HETEROGENEITY; HEREDITY; HUMAN; PRIORITY JOURNAL; TESTICULAR FEMINIZATION; X CHROMOSOMAL INHERITANCE;

EID: 0342597380     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.85.21.8151     Document Type: Article

References (0)