Genomic copy number alterations in non-syndromic hearing loss
Author:
Affiliation:
1. Department of Genetics and Evolutionary Biology, Institute of Bioscience; University of São Paulo; São Paulo Brazil
2. Department of Otorhinolaryngology, Medical School; University of São Paulo; São Paulo Brazil
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Chromosome imbalances in syndromic hearing loss;Catelani;Clin Genet,2009
2. Copy number variants are a common cause of non-syndromic hearing loss;Shearer;Genome Med,2014
3. An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH;Allemeersch;BMC Bioinformatics,2009
4. Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?;Silva;Eur J Hum Genet,2014
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