NGS of 13 gene panel: ASXL1, CACNA1C, CTNND2, EHMT1, IMMP2L, KANSL1, KCNK9, LIMK1, MYCN, SHANK3, RNF168, SATB2, TBX3

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Ref: LV3015 Categories: , , , , , , Diseases: Intellectual Disability syndromes, autosomal dominant: Bohring-Opitz; CRI-DU-CHAT; Gilles de la Tourette; Koolen-De Vries; Birk-Barel dysmorphism; Williams-Beuren; Feingold; Phelan-McDermid; RGenes: LIMK1, SATB2, KANSL1, MYCN, TBX3, CACNA1C, RNF168, KCNK9, CTNND2, ASXL1, EHMT1, IMMP2L, SHANK3Delivery term: 42 days