|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
9
|
|
pubmed:dateCreated |
2009-8-17
|
|
pubmed:abstractText |
Spontaneous premature ovarian failure (POF) occurs in 1% of women and has major implications for their fertility and health. Besides X chromosomal aberrations and fragile X premutations, no common genetic risk factor has so far been discovered in POF. Using high-density single nucleotide polymorphism (SNP) arrays, we set out to identify new genetic variants involved in this condition.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
1460-2350
|
|
pubmed:author |
pubmed-author:Christin-MaitreSophieS,
pubmed-author:Dutch POF Consortium,
pubmed-author:FauserBart C J MBC,
pubmed-author:FrankeLudeL,
pubmed-author:GoverdeAngelique JAJ,
pubmed-author:HoekAnnemiekeA,
pubmed-author:HsuehAaron JAJ,
pubmed-author:KnauffErik A HEA,
pubmed-author:LambalkCornelius BCB,
pubmed-author:LavenJoop S EJS,
pubmed-author:WijmengaCiscaC,
pubmed-author:van EsMichael AMA,
pubmed-author:van den BergLeonard HLH,
pubmed-author:van der SchouwYvonne TYT
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
24
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
2372-8
|
|
pubmed:dateRevised |
2010-11-18
|
|
pubmed:meshHeading |
|
|
pubmed:year |
2009
|
|
pubmed:articleTitle |
Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene.
|
|
pubmed:affiliation |
Department of Reproductive Medicine and Gynaecology, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands. knauff@gmail.com
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
