NGS of 16 gene panel: ASPM, CASC5, CASK, CDK19, CDK5RAP2, CENPJ, CEP135, CEP152, KIF11, MCPH1, PHC1, PNKP, STAMBP, STIL, WDR62, ZNF335.

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Documentation:
Ref: LV2987 Categories: , , , , , , , Diseases: Microcephaly (M) primary; M. with or without Chorioretinopathy, lymphedema, mental retardation; Mental retardation and M. with pontine and cerebellar hypoplasia; M. with capillary malformation syGenes: PNKP, ASPM, WDR62, CEP152, PHC1, STIL, STAMBP, CDK5RAP2, CASC5, KIF11, CASK, MCPH1, CENPJ, CDK19, CEP135, ZNF335Delivery term: 42 days
sistemas genómicos
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