Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia

Genes Chromosomes and Cancer

Volumn 20, Issue 1, 1997, Pages 73-81

  Gardiner, Anne C ^a   Corcoran, Martin M ^a   Oscier, David G ^a  

^a ROYAL BOURNEMOUTH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 13Q; CHROMOSOME TRANSLOCATION 13; CHRONIC LYMPHATIC LEUKEMIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 13; CYTOGENETICS; FEMALE; GENE EXPRESSION; GENES, RETINOBLASTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, LYMPHOCYTIC, CHRONIC; MALE; MICROSATELLITE REPEATS; TRANSLOCATION, GENETIC;

EID: 0030930177     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199709)20:1<73::AID-GCC11>3.0.CO;2-G     Document Type: Article

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