Identification of novel breast tumor-specific mutation(s) in the q11.2 region of chromosome 17 by RAPD/AP-PCR fingerprinting

Gene

Volumn 269, Issue 1-2, 2001, Pages 33-43

  Singh, Kamaleshwar P ^a   Roy, Deodutta ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Amplification; Arbitrary primer; Genetic instability; Polymorphism

Indexed keywords

ARTICLE; BREAST CARCINOMA; CARCINOGENESIS; CHROMOSOME 17; CHROMOSOME ARM; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; GENE AMPLIFICATION; GENE DELETION; GENE FREQUENCY; GENE INSERTION; GENE LOCATION; GENE LOCUS; GENOME; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

BREAST NEOPLASMS; CHROMOSOMES, HUMAN, PAIR 17; CLONING, MOLECULAR; DNA FINGERPRINTING; DNA, NEOPLASM; FEMALE; HOMOZYGOTE; HUMANS; LOSS OF HETEROZYGOSITY; MUTAGENESIS, INSERTIONAL; MUTATION; OPEN READING FRAMES; POLYMORPHISM, GENETIC; RANDOM AMPLIFIED POLYMORPHIC DNA TECHNIQUE; SEQUENCE DELETION;

EID: 0035897683     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(01)00458-9     Document Type: Article

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