Association between mutations of the follicle-stimulating-hormone receptor and repeated twinning

Lancet

Volumn 356, Issue 9233, 2000, Pages 914-

  Al Hendy, Ayman ^a   Moshynska, Oksana ^a   Saxena, Anurag ^a   Feyles, Valter ^a  

^a ROYAL UNIVERSITY HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

FOLLITROPIN; FOLLITROPIN RECEPTOR;

AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; DIZYGOTIC TWINS; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENOTYPE; HUMAN; OVARY FOLLICLE DEVELOPMENT; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; RESTRICTION SITE; TWIN PREGNANCY;

EID: 0034626074     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0140-6736(00)02687-8     Document Type: Article

References (3)

1. P Parisi M Gatti G Prinzi G Caperna Familial incidence of twinning Nature 304 1983 626 628
2. CB Lambalk DI Boomsma L de Boer Increased levels and pulsatility of follicle stimulating hormone in mothers of hereditary dizygotic twins J Clin Endocrinol Metab 83 1998 481 486
3. K Aittomaki JL Dieguez Lucena P Parkarinen Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure Cell 82 1995 959 968