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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
#612881 - CHROMOSOME 5q14.3 DELETION SYNDROME, DISTAL
Cytogenetic locations: 19876902
*600663 - MYOCYTE ENHANCER FACTOR 2D; MEF2D
Cytogenetic locations: 19119233
*600662 - MYOCYTE ENHANCER FACTOR 2C; MEF2C
*600661 - MYOCYTE ENHANCER FACTOR 2B; MEF2B
Cytogenetic locations: 600927
*600660 - MYOCYTE ENHANCER FACTOR 2A; MEF2A
Cytogenetic locations: 11516833
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