Common chromosomal fragile site FRA16D sequence: Identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Human Molecular Genetics

Volumn 9, Issue 11, 2000, Pages 1651-1663

  Ried, Karin ^a   Finnis, Merran ^a   Hobson, Lynne ^a   Mangelsdorf, Marie ^a   Dayan, Sonia ^a   Nancarrow, Julie K ^a   Woollatt, Erica ^a   Kremmidiotis, Gabriel ^a   Gardner, Alison ^a   Venter, Deon ^b   Baker, Elizabeth ^a   Richards, Robert I ^a  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^b PETER MACCALLUM CANCER CENTRE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; OXIDOREDUCTASE;

ALTERNATIVE RNA SPLICING; AMINO TERMINAL SEQUENCE; ARTICLE; CANCER CELL; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 16Q; CHROMOSOME BREAKAGE; CHROMOSOME FRAGILE SITE; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; DNA SEQUENCE; DNA STRUCTURE; DNA TRANSCRIPTION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GENE SEQUENCE; HOMOZYGOTE; HUMAN; HUMAN CELL; INTRON; MULTIPLE MYELOMA; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN;

EID: 17444440946     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.11.1651     Document Type: Article

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