Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7221
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dc.contributor.authorLower, K.en
dc.contributor.authorSolders, G.en
dc.contributor.authorBondeson, M.en
dc.contributor.authorNelson, J.en
dc.contributor.authorBrun, A.en
dc.contributor.authorCrawford, J.en
dc.contributor.authorMalm, G.en
dc.contributor.authorBorjeson, M.en
dc.contributor.authorTurner, G.en
dc.contributor.authorPartington, M.en
dc.contributor.authorGecz, J.en
dc.date.issued2004en
dc.identifier.citationEuropean Journal of Human Genetics, 2004; 12(10):787-789en
dc.identifier.issn1018-4813en
dc.identifier.issn1476-5438en
dc.identifier.urihttp://hdl.handle.net/2440/7221-
dc.description.statementofresponsibilityKaren M Lower, Göran Solders, Marie-Louise Bondeson, John Nelson, Arne Brun, Joanna Crawford, Gunilla Malm, Mats Börjeson, Gillian Turner, Michael Partington and Jozef Géczen
dc.language.isoenen
dc.publisherNature Publishing Groupen
dc.subjectHumans; Mental Retardation, X-Linked; Obesity; Hypogonadism; Syndrome; Arginine; Pedigree; Point Mutation; Female; Maleen
dc.title1024C>T (R342X) is a recurrent RHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome familyen
dc.title.alternative1024C>T (R342X) is a recurrent RHF6 mutation also found in the original Borjeson-Forssman-Lehmann syndrome familyen
dc.typeJournal articleen
dc.identifier.rmid0020041839en
dc.identifier.doi10.1038/sj.ejhg.5201228en
dc.identifier.pubid56001-
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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