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Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability

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Description scientific article
Author/s

author: Lucile Pinson  Jean Donadieu  Delphine Héron  Christine Bellanné-Chantelot  Ange-Line Bruel 

Publication date September 12, 2016
Language English
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