Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns

Genome Medicine

Volumn 4, Issue 10, 2012, Pages

  Coughlin II, Curtis R ^a   Scharer, Gunter H ^a,b   Shaikh, Tamim H ^a,b  

^a Children's Hospital Colorado   (United States)

^b UNIVERSITY OF COLORADO   (United States)

Author keywords

CGH; CNV; Comparative genomic hybridization; copy number variation; genetic counseling; microarray; single nucleotide polymorphism; SNP

Indexed keywords

CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; FAMILY; GENE MUTATION; GENETIC COUNSELING; GENOMIC INSTABILITY; HEALTH CARE PERSONNEL; HUMAN; LABORATORY; MEDICAL DECISION MAKING; MICROARRAY ANALYSIS; PHENOTYPE; PRENATAL PERIOD; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84867895156     PISSN: None     EISSN: 1756994X     Source Type: Journal    
DOI: 10.1186/gm381     Document Type: Review

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