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Carter, Nigel P

TitleYearPMID
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. 2011 21552272
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. 2010 20466091
Origins and functional impact of copy number variation in the human genome. 2010 19812545
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. 2009 19344873
A second generation human haplotype map of over 3.1 million SNPs. 2007 17943122
Diet and the evolution of human amylase gene copy number variation. 2007 17828263
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