Electrophoretic microfluidic devices for mutation detection in clinical diagnostics

Expert Opinion on Medical Diagnostics

Volumn 2, Issue 8, 2008, Pages 963-977

  Dewald, Alison H ^a   Poe, Brian L ^a   Landed, James P ^a,b,c  

^a UNIVERSITY OF VIRGINIA   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c University of Virginia   (United States)

Author keywords

Allele specific PCR; Electrophoresis; Heteroduplex analysis; Microchip; Microfluidic; Mutation detection; Polymorphism; Restriction fragment length polymorphism; Single strand conformational polymorphism

Indexed keywords

BIOLOGICAL MARKER; GENOMIC DNA; METHYLPHENIDATE; MITOCHONDRIAL DNA; POLYACRYLAMIDE; POLYMER; SEROTONIN TRANSPORTER;

ALLELE; ANTHRAX; COLORECTAL CANCER; COMPUTER SYSTEM; DIAGNOSTIC VALUE; DNA METHYLATION; DNA POLYMORPHISM; EARLY DIAGNOSIS; ELECTROPHORETIC MICROFLUIDIC DEVICE; ENZYME ASSAY; FAMILIAL HYPERCHOLESTEROLEMIA; FRAGILE X SYNDROME; GENE MUTATION; GENETIC ANALYSIS; GENETIC MARKER; GENOME SIZE; GENOTYPE; HETERODUPLEX ANALYSIS; HUMAN; HUMAN GENOME PROJECT; HYPERHOMOCYSTEINEMIA; LAB ON A CHIP; LABORATORY APPARATUS, EQUIPMENT AND SUPPLIES; MICROCHIP ELECTROPHORESIS; MITOCHONDRIAL ENCEPHALOPATHY; MULTIPLEX POLYMERASE CHAIN REACTION; MUTATIONAL ANALYSIS; NEURAL TUBE DEFECT; NONHUMAN; PERIPHERAL OCCLUSIVE ARTERY DISEASE; PERTUSSIS; POINT OF CARE TESTING; POLYMERASE CHAIN REACTION; PROGNOSIS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; REVIEW; SINGLE STRAND CONFORMATION POLYMORPHISM; T CELL LYMPHOMA; VALIDATION PROCESS;

EID: 77953378955     PISSN: 17530059     EISSN: 17530067     Source Type: Journal    
DOI: 10.1517/17530059.2.8.963     Document Type: Review

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