WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. (Q55692902)

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scientific article published on 17 September 2012
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WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype.
scientific article published on 17 September 2012

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    WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. (English)

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