Genotyping of frequent BRCA1/2 SNPs with unlabeled probes: A supplement to HRMCA mutation scanning, allowing the strong reduction of sequencing burden

Journal of Molecular Diagnostics

Volumn 11, Issue 5, 2009, Pages 415-419

  De Leeneer, Kim ^a   Coene, Ilse ^a   Poppe, Bruce ^a   De Paepe, Anne ^a   Claes, Kathleen ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN;

ARTICLE; DNA PROBE; GENE MUTATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; ONCOGENE; POLYMERASE CHAIN REACTION; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM;

APOPTOSIS REGULATORY PROTEINS; BRCA1 PROTEIN; BRCA2 PROTEIN; DNA MUTATIONAL ANALYSIS; GENOTYPE; HUMANS; MUTATION; OLIGONUCLEOTIDE PROBES; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 70249138056     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.2353/jmoldx.2009.090032     Document Type: Article

References (9)

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