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    Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome 
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    • Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome
    •   QMRO Home
    • Blizard Institute
    • Centre for Genomics and Child Health
    • Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome
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    Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome

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    WALNEMutationsIn2010POSTP.doc (196Kb)
    WALNEMutationsIn2010POSTP-tables.doc (63Kb)
    Volume
    19
    Pagination
    4453 - 4461
    DOI
    10.1093/hmg/ddq371
    Journal
    HUM MOL GENET
    Issue
    22
    ISSN
    0964-6906
    Metadata
    Show full item record
    Authors
    Walne, AJ; Vulliamy, T; Beswick, R; Kirwan, M; Dokal, I
    URI
    http://qmro.qmul.ac.uk/xmlui/handle/123456789/2300
    Collections
    • Centre for Genomics and Child Health [683]
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