17p- Syndrome arising from a novel dicentric translocation in a patient with acute myeloid leukemia

Cancer Genetics and Cytogenetics

Volumn 118, Issue 2, 2000, Pages 159-162

  Watson, Neville ^a   Dunlop, Lindsay ^b   Robson, Lisa ^a   Sharma, Praveen ^a   Smith, Arabella ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b LIVERPOOL HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; AGED; ARTICLE; CASE REPORT; CHROMOSOME 17P; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; DYSPLASIA; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; HUMAN CELL; KARYOTYPE; LEUKOCYTE DISORDER; MALE; PRIORITY JOURNAL; SYNDROME; THROMBOCYTOPENIA;

AGED; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 20; FOLLOW-UP STUDIES; HUMANS; KARYOTYPING; LEUKEMIA, MYELOCYTIC, ACUTE; MALE; SYNDROME; TRANSLOCATION, GENETIC;

EID: 0034655535     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00188-0     Document Type: Article

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