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Autosomal dominant "non-syndromic" intellectual disability
- ... a characteristic facial appearance, delayed growth and development, intellectual disability, and seizures. A loss of the MSX1 gene ... Lin BP, Hu JC. Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res. 2006 Mar;85(3): ...
- ... NODAL TDGF1 Nonsyndromic holoprosencephaly is inherited in an autosomal dominant pattern, which means an alteration in one copy ...