Your browser doesn't support javascript.
loading
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Genome Res ; 23(9): 1395-409, 2013 Sep.
Article in En | MEDLINE | ID: mdl-23657883

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Disorders / Alleles / DNA Copy Number Variations / Homologous Recombination / Genetic Diseases, Inborn Limits: Humans Language: En Journal: Genome Res Journal subject: BIOLOGIA MOLECULAR / GENETICA Year: 2013 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Disorders / Alleles / DNA Copy Number Variations / Homologous Recombination / Genetic Diseases, Inborn Limits: Humans Language: En Journal: Genome Res Journal subject: BIOLOGIA MOLECULAR / GENETICA Year: 2013 Document type: Article Affiliation country: United States Country of publication: United States