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#619480 - NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND THIN CORPUS CALLOSUM; NEDDFAC
Cytogenetic locations: mutation
Gene summaries Genetic tests Medical literature
#613457 - CHROMOSOME 14q11-q22 DELETION SYNDROME
Cytogenetic locations: 610041
*609904 - HISTONE GENE CLUSTER 1, H2B HISTONE FAMILY, MEMBER A; HIST1H2BA
Cytogenetic locations: 12213818
*609798 - NIMA-RELATED KINASE 9; NEK9
Cytogenetic locations: 614528
*605012 - SPT16 HOMOLOG, FACILITATES CHROMATIN REMODELING SUBUNIT; SUPT16H
*604328 - STRUCTURE-SPECIFIC RECOGNITION PROTEIN 1; SSRP1
Cytogenetic locations: 10336466
*603375 - SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 5; SMARCA5
Cytogenetic locations: 17099699
*191170 - TUMOR PROTEIN p53; TP53
Cytogenetic locations: 27997263
*115442 - CASEIN KINASE II, ALPHA-2; CSNK2A2
Cytogenetic locations: 151510
*115441 - CASEIN KINASE II, BETA; CSNK2B
Cytogenetic locations: 22276748
*115440 - CASEIN KINASE II, ALPHA-1; CSNK2A1
Cytogenetic locations: 21766873
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