Frequency of new copy number variation in humans
By G. V. Ommen. Nature Genetics, 2005
104 citations recorded by the source corpus.
Subfields: Genetics, Pediatrics, Perinatology and Child Health
View Paper: https://www.semanticscholar.org/paper/a86047f08b4406bae2adece99f28e11b162863e1
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In Genetics
In Pediatrics, Perinatology and Child Health
Citations in the corpus
- Copy-number variations associated with neuropsychiatric conditions (2008, background): “First, family data suggest a comparatively high locus-specific rate of new nucleotide mutation in CNVs, three to four times that for SNP”