A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies

Cancer Genetics and Cytogenetics

Volumn 163, Issue 2, 2005, Pages 176-179

  MacKinnon, Ruth N ^a   Campbell, Lynda J ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; AGED; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 20; CHROMOSOME 20Q; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME DELETION 20; CHROMOSOME DUPLICATION; COMPARATIVE STUDY; FEMALE; HUMAN; HUMAN CELL; ISOCHROMOSOME; MORPHOLOGY; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; PRIORITY JOURNAL;

AGED; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; KARYOTYPING; MYELODYSPLASTIC SYNDROMES;

EID: 28744458516     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2005.06.001     Document Type: Article

References (11)

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