A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome

E-ISSN： 1098-1004|36|11|1043-1047

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.36, Iss.11, 2015-11, pp. : 1043-1047

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