Copy-number variation and association studies of human disease

Nature Genetics

Volumn 39, Issue 7S, 2007, Pages S37-S42

  McCarroll, Steven A ^a,b   Altshuler, David M ^a,b  

^a BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; DISEASE ASSOCIATION; GENE NUMBER; GENOTYPE; HUMAN; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

BIAS (EPIDEMIOLOGY); GENE DOSAGE; GENETIC DISEASES, INBORN; GENETICS, MEDICAL; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; VARIATION (GENETICS);

EID: 34347353237     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng2080     Document Type: Article

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