Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder

Genes Chromosomes and Cancer

Volumn 21, Issue 1, 1998, Pages 70-73

  Smedley, Damian ^a   Somers, Gino ^b   Venter, Deon ^b   Chow, Chung Wo ^c   Cooper, Colin ^a   Shipley, Janet ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b PETER MACCALLUM CANCER CENTRE   (Australia)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 13P; CHROMOSOME 8P; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 8; CLINICAL ARTICLE; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LEUKEMOGENESIS; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 8; HUMANS; KARYOTYPING; METAPHASE; MYELOPROLIFERATIVE DISORDERS; NUCLEIC ACID HYBRIDIZATION; TRANSLOCATION, GENETIC;

EID: 0031984252     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199801)21:1<70::AID-GCC9>3.0.CO;2-5     Document Type: Article

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