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dc.contributor.authorMorgan, NVen_US
dc.contributor.authorGissen, Pen_US
dc.contributor.authorSharif, SMen_US
dc.contributor.authorBaumber, Len_US
dc.contributor.authorSutherland, Jen_US
dc.contributor.authorKelly, DAen_US
dc.contributor.authorAminu, Ken_US
dc.contributor.authorBennett, CPen_US
dc.contributor.authorWoods, CGen_US
dc.contributor.authorMueller, RFen_US
dc.contributor.authorTrembath, RCen_US
dc.contributor.authorMaher, ERen_US
dc.contributor.authorJohnson, CAen_US
dc.date.accessioned2015-05-20T12:06:57Z
dc.date.available2002-07-12en_US
dc.date.issued2002-10en_US
dc.identifier.issn0340-6717en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/7466
dc.format.extent456 - 461en_US
dc.relation.ispartofHUM GENETen_US
dc.subjectNEURAL-TUBE DEFECTSen_US
dc.subjectMALFORMATIONSen_US
dc.subjectHETEROGENEITYen_US
dc.subjectANOMALIESen_US
dc.subjectSPECTRUMen_US
dc.subjectCHILDRENen_US
dc.subjectDISEASEen_US
dc.subjectDNAen_US
dc.titleA novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24en_US
dc.typeArticle
dc.identifier.doi10.1007/s00439-002-0817-0en_US
pubs.issue4-5en_US
pubs.notesNot knownen_US
pubs.volume111en_US


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