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dc.contributor.authorTurnpenny, Peter D.en
dc.date.accessioned2018-12-20T13:55:53Z
dc.date.available2018-12-20T13:55:53Z
dc.date.issued2018-12-14
dc.identifier.citationPiña-Aguilar RE, Simpson SA, Alshatti A, et al. 27 years of prenatal diagnosis for Huntington disease in the United Kingdom. Genet Med. 2019;21(7):1639-1643. doi:10.1038/s41436-018-0367-z. Epub 2018 Dec 14en
dc.identifier.issn1530-0366
dc.identifier.pmid30546084
dc.identifier.doi10.1038/s41436-018-0367-z
dc.identifier.urihttp://hdl.handle.net/11287/620936
dc.description.abstractThere is little long-term, population-based data on uptake of prenatal diagnosis for Huntington disease (HD), a late-onset autosomal dominant neurodegenerative disorder, and the effect of the availability of preimplantation genetic diagnosis (PGD) on families' decisions about conventional prenatal diagnosis is not known. We report trends in prenatal diagnosis and preimplantation diagnosis for HD in the United Kingdom since services commenced.en
dc.language.isoenen
dc.publisherNatureen
dc.relation.urlhttp://dx.doi.org/10.1038/s41436-018-0367-zen
dc.rightsArchived with thanks to Genetics in medicine : official journal of the American College of Medical Geneticsen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.title27 years of prenatal diagnosis for Huntington disease in the United Kingdom.en
dc.typeJournal Articleen
dc.identifier.journalGenetics in medicine : official journal of the American College of Medical Geneticsen
dc.type.versionPublisheden


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