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CharGer: clinical Characterization of Germline variants
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WebSep 5, 2024 · The cause of CHARGE is usually a new mutation (change) in the CHD7 gene, or rarely, genomic alterations in the region of chromosome 8q12.2 where the CHD7 gene is located. Among 119 French children with CHARGE syndrome, CHD7 mutations were found in 83% of typical CHARGE syndrome individuals, and 58% of atypical cases. WebJun 7, 2024 · A gene associated with CHARGE syndrome has been identified on chromosome 8 and involves mutations of the CHD7 gene (the CHD7 gene is the only … WebApr 7, 2024 · ORIgen is a proud partner of Allied Genetic Resources. owned by breeders, that have united to help both groups of breeders market their Master Breeder Genetics. Through this partnership, you as... trade now app