Are FSHR polymorphisms risk factors to premature ovarian insufficiency?

Gynecological Endocrinology

Volumn 31, Issue 8, 2015, Pages 663-666

  Cordts, Emerson Barchi ^a   Santos, Monise Castro ^a   Bianco, Bianca ^a   Barbosa, Caio Parente ^a   Christofolini, Denise Maria ^a  

^a FACULDADE DE MEDICINA DO ABC   (Brazil)

Author keywords

Follicle stimulating hormone; FSHR; infertility; premature ovarian insufficiency; X chromosome

Indexed keywords

FOLLITROPIN; FOLLITROPIN RECEPTOR;

ADULT; ALLELE; ARTICLE; CHROMOSOME ANALYSIS; CONTROLLED STUDY; FEMALE; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; MENOPAUSE; PREMATURE OVARIAN FAILURE; PRIORITY JOURNAL; X CHROMOSOME; BLOOD; EARLY MENOPAUSE; GENE FREQUENCY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; YOUNG ADULT;

ADULT; ALLELES; FEMALE; FOLLICLE STIMULATING HORMONE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MENOPAUSE, PREMATURE; POLYMORPHISM, SINGLE NUCLEOTIDE; PRIMARY OVARIAN INSUFFICIENCY; RECEPTORS, FSH; RISK FACTORS; YOUNG ADULT;

EID: 84942830570     PISSN: 09513590     EISSN: 14730766     Source Type: Journal    
DOI: 10.3109/09513590.2015.1032933     Document Type: Article

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