Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/23247
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dc.contributor.authorCrawford, J.en
dc.contributor.authorLower, K.en
dc.contributor.authorHennekam, R.en
dc.contributor.authorVan Esch, H.en
dc.contributor.authorMegarbane, A.en
dc.contributor.authorLynch, S.en
dc.contributor.authorTurner, G.en
dc.contributor.authorGecz, J.en
dc.date.issued2006en
dc.identifier.citationJournal of Medical Genetics, 2006; 43(3):238-243en
dc.identifier.issn0022-2593en
dc.identifier.issn1468-6244en
dc.identifier.urihttp://hdl.handle.net/2440/23247-
dc.descriptioncopyright © 2006 by the BMJ Publishing Group Ltd.en
dc.description.abstractObjective: To present the results of mutation screening in individuals referred for PHF6 testing and discuss the value of prior X-inactivation testing in the mothers of these individuals. Results: 25 unrelated individuals were screened (24 male, one female). Five PHF6 mutations were detected, two of which (c.940A->G and c.27_28insA) were novel. One of these new mutations, c.27_28insA, was identified in a female BFLS patient. This was shown to be a de novo mutation arising on the paternal chromosome. This is the first report of a clinically diagnosed BFLS female with a confirmed PHF6 mutation. In addition, the X-inactivation status of the mothers of 19 males with suggested clinical diagnosis of BFLS was determined. Skewed (>=70%) X-inactivation was present in five mothers, three of whom had sons in whom a PHF6 mutation was detected. The mutation positive female also showed skewing. Conclusions: The results indicate that the success of PHF6 screening in males suspected of having BFLS is markedly increased if there is a positive family history and/or skewed X-inactivation is found in the mother. Abbreviations: AR, androgen receptor; BFLS, Börjeson-Forssman-Lehmann syndrome; ORF, open reading frame; XLMR, X linked mental retardationen
dc.language.isoenen
dc.publisherBritish Med Journal Publ Groupen
dc.subjectBFLS; PHF6; mutation summary; skewed X-inactivationen
dc.titleMutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patienten
dc.typeJournal articleen
dc.identifier.rmid0020060207en
dc.identifier.doi10.1136/jmg.2005.033084en
dc.identifier.pubid53153-
pubs.library.collectionPaediatrics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

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