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#619092 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES; NEDMILEG
Cytogenetic locations: 32738225
Gene summaries Genetic tests Medical literature
#619091 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, AND GAIT ABNORMALITIES; NEDMILG
Cytogenetic locations: 32788587
*612282 - ZINC FINGER PROTEIN 804A; ZNF804A
Cytogenetic locations: 16713569
*612149 - RNA-BINDING FOX1 HOMOLOG 2; RBFOX2
Cytogenetic locations: 617620
*609590 - QKI, KH DOMAIN-CONTAINING RNA-BINDING PROTEIN; QKI
Cytogenetic locations: 11917126
*609526 - PLECKSTRIN HOMOLOGY DOMAIN- AND RhoGEF DOMAIN-CONTAINING PROTEIN G4; PLEKHG4
Cytogenetic locations: 16491300
*607462 - ATROPHIN 1; ATN1
Cytogenetic locations: 607528
*605104 - RNA-BINDING FOX1 HOMOLOG 1; RBFOX1
Cytogenetic locations: 30318414
*601558 - RNA-BINDING PROTEIN, mRNA-PROCESSING FACTOR; RBPMS
Cytogenetic locations: 18855282
*601556 - ATAXIN 1; ATXN1
ATXN1, ALTERNATIVE READING FRAME, INCLUDED
Cytogenetic locations: 603453
*601517 - ATAXIN 2; ATXN2
Cytogenetic locations: 23687048
*600272 - COILIN; COIL
Cytogenetic locations: 11470819
*108410 - ASPARAGINYL-tRNA SYNTHETASE 1; NARS1
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