cgh-array analysis (Agilent technologies)
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Cgh Array Analysis, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/array+cgh+analysis/pm28480548-46-10-5
Average 90 stars, based on 1 article reviews
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other:Article Title: Expanding the phenotypic spectrum of truncating POGZ mutations: Association with CNS malformations, skeletal abnormalities, and distinctive facial dysmorphism. Article Snippet: Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy Correspondence Maria Lisa Dentici, MD, Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Viale di San Paolo, 15, 00146 Rome, Italy.. Email: marialisa.dentici@opbg.net Funding information (Vite Coraggiose to M.T.); (GeneRare to B.D.); (RC2017, to M.N., M.L.D. and M.T.); CINECA (computational resources, to M.T.). Exome sequencing has led to the comprehension of the molecular bases of several forms of neurodevelopmental disorders, a clinically heterogeneous group of diseases characterized by intellectual disability (ID) and autism spectrum disorder (ASD). |
