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A novel RAD21 variant associated with intrafamilial phenotypic variation in Cornelia de Lange syndrome - review of the literature

CLINICAL GENETICS (2017)

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Journal

CLINICAL GENETICS
Volume 91, Issue 4, Pages 647-649

Publisher

WILEY
DOI: 10.1111/cge.12863

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Categories

Genetics & Heredity

Funding

  1. A.P. Moller and wife Chastine Mc-Kinney Mollers Foundation

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