Last Updated: 09/26/2026
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Found 2 publications
De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features.
Journal: American journal of medical genetics. Part A
Published: March 19, 2018
POGZ truncating alleles cause syndromic intellectual disability.
Journal: Genome medicine
Published: August 04, 2015
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Last Updated: 09/26/2026