Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning

Lancet

Volumn 357, Issue 9258, 2001, Pages 773-774

  Montgomery, Grant W ^a,d   Duffy, David L ^a   Hall, Jeff ^b   Kudo, Masataka ^c   Martin, Nicholas G ^a   Hsueh, Aaron J ^c  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b PPGx Inc   (United States)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

^d ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FOLLITROPIN; HORMONE RECEPTOR; MUTANT PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 2; DIZYGOTIC TWINS; DNA FLANKING REGION; GENETIC ANALYSIS; HUMAN; MUTATION; PEDIGREE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TWIN PREGNANCY;

EID: 0035836004     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)04164-7     Document Type: Article

References (5)

1. Genetic modelling of dizygotic twinning in pedigrees of spontaneous dizygotic twins
2. Dizygotic twinning is not linked to variation at the α-inhibin locus on human chromosome 2
3. Association between mutations of the follicle-stimulating-hormone receptor and repeated twinning
4. Ovarian response to follicle-stimulating hormone (FSH) stimulation depends on the FSH receptor genotype