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Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

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dc.creatorOjeda D.spa
dc.creatorLakhal B.spa
dc.creatorFonseca Mendoza, Dora Janethspa
dc.creatorBraham R.spa
dc.creatorLandolsi H.spa
dc.creatorMateus H.E.spa
dc.creatorRestrepo Fernández, Carlos Martínspa
dc.creatorElghezal H.spa
dc.creatorSaâd A.spa
dc.creatorLaissue P.spa
dc.date.accessioned2020-05-26T00:08:09Z
dc.date.available2020-05-26T00:08:09Z
dc.date.created2011spa
dc.description.abstractEarlier 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. © 2011 by American Society for Reproductive Medicine.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1016/j.fertnstert.2011.04.045
dc.identifier.issn150282
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/24059
dc.language.isoengspa
dc.publisherElsevier Inc.spa
dc.relation.citationEndPage2660.e1
dc.relation.citationIssueNo. 8
dc.relation.citationStartPage2658
dc.relation.citationTitleFertility and Sterility
dc.relation.citationVolumeVol. 95
dc.relation.ispartofFertility and Sterility, ISSN:150282, Vol.95, No.8 (2011); pp. 2658-2660.e1spa
dc.relation.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-79959751824&doi=10.1016%2fj.fertnstert.2011.04.045&partnerID=40&md5=28ecf0ec8b9d87ed20486bc697a85953spa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto Completo)spa
dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subject.keywordCyclin dependent kinase inhibitor 1Bspa
dc.subject.keywordFollitropinspa
dc.subject.keywordAdultspa
dc.subject.keywordArticlespa
dc.subject.keywordAutoimmune diseasespa
dc.subject.keywordControlled studyspa
dc.subject.keywordFemalespa
dc.subject.keywordFemale infertilityspa
dc.subject.keywordFollitropin blood levelspa
dc.subject.keywordGene mutationspa
dc.subject.keywordGenetic analysisspa
dc.subject.keywordGenetic codespa
dc.subject.keywordHumanspa
dc.subject.keywordInformed consentspa
dc.subject.keywordKaryotypespa
dc.subject.keywordMajor clinical studyspa
dc.subject.keywordOvary developmentspa
dc.subject.keywordOvary insufficiencyspa
dc.subject.keywordPelvis surgeryspa
dc.subject.keywordPhenotypespa
dc.subject.keywordPremature ovarian failurespa
dc.subject.keywordPriority journalspa
dc.subject.keywordSequence analysisspa
dc.subject.keywordSingle nucleotide polymorphismspa
dc.subject.keywordCDKN1Bspa
dc.subject.keywordMutationsspa
dc.subject.keywordPremature ovarian failure (POF)spa
dc.subject.keywordSequencingspa
dc.titleSequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotypespa
dc.typearticleeng
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.type.spaArtículospa
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