A paradigm for finding genes for a complex human trait: Polycystic ovary syndrome and follistatin

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

Volumn 96, Issue 15, 1999, Pages 8315-8317

  Odunsi, K ^a   Kidd, K K ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FOLLISTATIN; FOLLITROPIN; LUTEINIZING HORMONE;

CLINICAL FEATURE; DNA POLYMORPHISM; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HYPERANDROGENISM; MARKER GENE; NOTE; OVARY POLYCYSTIC DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; SIGNAL TRANSDUCTION;

ALLELES; CHROMOSOME MAPPING; CLONING, MOLECULAR; FEMALE; FOLLICLE STIMULATING HORMONE; FOLLISTATIN; GENETIC MARKERS; GLYCOPROTEINS; HUMANS; HYPERANDROGENISM; LINKAGE (GENETICS); LUTEINIZING HORMONE; NUCLEAR FAMILY; OVARY; PHENOTYPE; POLYCYSTIC OVARY SYNDROME;

EID: 0033587706     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.15.8315     Document Type: Note

References (31)