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By Balicky Eric   Young Lynn   Orr-Weaver Terry   Bickel Sharon  

Chromosoma, Vol. 112, Iss. 5, 2004-02 ,pp. : 231-239

Springer Publishing Company

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Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and RothmundThomson syndrome

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Oxford University Press

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Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene

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John Wiley & Sons Inc

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Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes

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INCENP loss from an inactive centromere correlates with the loss of sister chromatid cohesion

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