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Clinical and molecular genetic characterization of a male patient with Sensenbrenner syndrome (cranioectodermal dysplasia) and biallelic WDR35 mutations

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Description scientific article published on 14 November 2017
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author: Katarzyna Zachwieja  Magdalena Socha  Anna Swiader  Anna Wawrocka  Joanna Walczak-Sztulpa  Anna Latos-Bieleńska  Aleksander Jamsheer 

Publication date November 14, 2017
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