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

Consult

Documentation:
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
sistemas genómicos
Privacy Summary

This website uses cookies so that we can offer you the best possible user experience. Cookie information is stored in your browser and performs functions such as recognizing you when you return to our website or helping our team understand which sections of the website you find most interesting and useful. You can access our privacy policy here