Linked Life Data

21575944

Source:http://linkedlifedata.com/resource/pubmed/id/21575944

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2011-6-27
pubmed:abstractText
Earlier reports demonstrated a key role of Cdkn1b during mouse ovarian development. In this study, the sequencing analysis of the complete coding region of this gene in a panel of premature ovarian failure patients and control subjects reveals a novel mutation potentially related to the phenotype.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1556-5653
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
30
pubmed:volume
95
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2658-60.e1
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype.
pubmed:affiliation
Unidad de Genética, Escuela de Medicina y Ciencias de la Salud, Universidad del Rosario, Bogotá, Colombia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study