TY  - GEN
AU  - Layman,L C
AU  - Amde,S
AU  - Cohen,D P
AU  - Jin,M
AU  - Xie,J
TI  - The Finnish follicle-stimulating hormone receptor gene mutation is rare in North American women with 46,XX ovarian failure
SN  - 0015-0282
PY  - 1998///0324
KW  - Adolescent
KW  - Adult
KW  - Alleles
KW  - DNA
KW  - analysis
KW  - Diploidy
KW  - Electrophoresis, Polyacrylamide Gel
KW  - Ethnicity
KW  - Female
KW  - Finland
KW  - Humans
KW  - North America
KW  - Point Mutation
KW  - genetics
KW  - Polymerase Chain Reaction
KW  - Primary Ovarian Insufficiency
KW  - ethnology
KW  - Receptors, FSH
N1  - Publication Type: Comparative Study; Journal Article
UR  - https://doi.org/10.1016/s0015-0282(97)00480-9
ER  -