Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|6|1414-1417

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.6, 2015-06, pp. : 1414-1417

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