Show simple item record

dc.contributor.authorWalne, AJen_US
dc.contributor.authorVulliamy, Ten_US
dc.contributor.authorBeswick, Ren_US
dc.contributor.authorKirwan, Men_US
dc.contributor.authorDokal, Ien_US
dc.date.accessioned2011-02-10T14:05:23Z
dc.date.accessioned2011-11-15T15:49:53Z
dc.date.issued2010-11-15en_US
dc.identifier.issn0964-6906en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/2300
dc.descriptionThis is a pre-copy-editing, author-produced PDF of an article accepted for publication in Human Molecular Genetics following peer review. The definitive publisher-authenticated version [Hum Mol Genet 19(22):4453-4461] is available online at: http://hmg.oxfordjournals.org/content/19/22/4453.full.pdf+htmlen_US
dc.format.extent4453 - 4461en_US
dc.relation.ispartofHUM MOL GENETen_US
dc.relation.replaceshttps://qmro.qmul.ac.uk/jspui/handle/123456789/632
dc.relation.replaces123456789/632
dc.subjectCLERICUZIO-TYPE POIKILODERMAen_US
dc.subjectCOMPONENTen_US
dc.subjectGENEen_US
dc.subjectNAVAJOen_US
dc.subjectFAMILYen_US
dc.subjectTINF2en_US
dc.titleMutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndromeen_US
dc.typeArticle
dc.identifier.doi10.1093/hmg/ddq371en_US
pubs.issue22en_US
pubs.notesNot knownen_US
pubs.volume19en_US


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record