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dc.contributor.authorOchando, Isabel-
dc.contributor.authorAlonzo Martínez, Melanie Cristine-
dc.contributor.authorSerrano, Ana María-
dc.contributor.authorUrbano, Antonio-
dc.contributor.authorCazorla, Eduardo-
dc.contributor.authorCalvo, Dolores-
dc.contributor.authorRueda, Joaquín-
dc.contributor.otherDepartamentos de la UMH::Histología y Anatomíaes_ES
dc.date.accessioned2025-10-31T09:40:33Z-
dc.date.available2025-10-31T09:40:33Z-
dc.date.created2018-07-
dc.identifier.citationThe application of clinical genetics. 2018 Jul 3:11:77-80es_ES
dc.identifier.issn1178-704X-
dc.identifier.urihttps://hdl.handle.net/11000/37755-
dc.description.abstractReported cases of distal 15q interstitial duplications are uncommon and do not result in a recognizable pattern of abnormalities. Some studies report prenatal overgrowth, while others describe growth retardation. We present molecular cytogenetic characterization of a 14 Mb interstitial duplication, encompassing 81 Online Mendelian Inheritance in Man (OMIM) genes, in a fetus with single umbilical artery and short limbs. We propose that growth restriction, previously described and present in our patient, may be due to duplication of a gene or genes contained in the 15q24 region.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent4es_ES
dc.language.isoenges_ES
dc.publisherTaylor and Francis. Group Dove Presses_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectdistal 15q trisomyes_ES
dc.subjectprenatal diagnosises_ES
dc.subjectshort limbses_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes_ES
dc.titlePrenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.2147/TACG.S159377es_ES
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Artículos Histología y Anatomía


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