Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2005-1-25
pubmed:abstractText
Women who carry the FMR1 premutation allele have a significantly increased risk for ovarian dysfunction. We hypothesize that molecular characteristics of the FMR1 gene may explain this increased risk.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0268-1161
pubmed:author
pubmed:issnType
Print
pubmed:volume
20
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
402-12
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15608041-Adolescent, pubmed-meshheading:15608041-Adult, pubmed-meshheading:15608041-Age Distribution, pubmed-meshheading:15608041-Aged, pubmed-meshheading:15608041-Dosage Compensation, Genetic, pubmed-meshheading:15608041-Female, pubmed-meshheading:15608041-Follicle Stimulating Hormone, pubmed-meshheading:15608041-Fragile X Mental Retardation Protein, pubmed-meshheading:15608041-Genetic Predisposition to Disease, pubmed-meshheading:15608041-Genomic Imprinting, pubmed-meshheading:15608041-Humans, pubmed-meshheading:15608041-Menopause, Premature, pubmed-meshheading:15608041-Middle Aged, pubmed-meshheading:15608041-Nerve Tissue Proteins, pubmed-meshheading:15608041-Prevalence, pubmed-meshheading:15608041-Primary Ovarian Insufficiency, pubmed-meshheading:15608041-RNA-Binding Proteins, pubmed-meshheading:15608041-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:15608041-Risk Factors
pubmed:year
2005
pubmed:articleTitle
Association of FMR1 repeat size with ovarian dysfunction.
pubmed:affiliation
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, N.I.H., Extramural