Human microcephaly

This publication has 45 references indexed in Scilit:

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• A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2
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• Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation
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• Mutant deoxynucleotide carrier is associated with congenital microcephaly
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• Clinical and genetic heterogeneity of Seckel syndrome
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• Primary Autosomal Recessive Microcephaly: MCPH5 Maps to 1q25-q32
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