4 results on '"Boycott KM"'
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2. P.131 De novo PIK3CB mutation associated with macrocephaly and diffuse polymicrogyria
3. P.070 Autosomal dominant MARS mutation linked to severe early onset CMT2U
4. A founder mutation inBBS2is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders
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