Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays

Cytogenetic and Genome Research

Volumn 123, Issue 1-4, 2009, Pages 322-332

  Winchester, L ^a   Newbury, D F ^a   Monaco, A P ^a   Ragoussis, J ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 16; CHROMOSOME BREAKAGE; CONTROLLED STUDY; GENE; GENE DELETION; GENE LOCATION; GENETIC LINKAGE; GENETIC VARIABILITY; HUMAN; HUMAN GENOME; INTRON; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; WWOX GENE;

BASE SEQUENCE; CELL LINE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; DATABASES, GENETIC; DNA; DNA DAMAGE; GENE DOSAGE; GENOME, HUMAN; HUMANS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 62549151335     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000184724     Document Type: Article

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