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#613443 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL
CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL, INCLUDED
Cytogenetic locations: MRPS27
Gene summaries Genetic tests Medical literature
*600662 - MYOCYTE ENHANCER FACTOR 2C; MEF2C
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