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*611000 - ENHANCER OF POLYCOMB HOMOLOG 2; EPC2
Gene summaries Genetic tests Medical literature
*603056 - ORIGIN RECOGNITION COMPLEX, SUBUNIT 4; ORC4
Cytogenetic locations: #B####
#613800 - MEIER-GORLIN SYNDROME 2; MGORS2
Cytogenetic locations: #!#t##
#615282 - CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2
Cytogenetic locations: -
*604593 - KINESIN FAMILY MEMBER 5C; KIF5C
*611472 - METHYL-CpG-BINDING DOMAIN PROTEIN 5; MBD5
#156200 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 1; MRD1
CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED
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