Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-)

British Journal of Haematology

Volumn 125, Issue 3, 2004, Pages 337-342

  Li, Tianyu ^a   Xue, Yongquan ^a   Wu, Yafang ^a   Pan, Jinlan ^a  

^a THE FIRST AFFILIATED HOSPITAL OF SOOCHOW UNIVERSITY   (China)

Author keywords

Deletion of 20q; Fluorescence in situ hybridization; Isochromosome; Myeloid disease; Prognosis

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; BONE MARROW CULTURE; CANCER SURVIVAL; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME G BAND; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CHROMOSOME R BAND; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; SURVIVAL RATE; TELOMERE;

AGED; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; KARYOTYPING; LEUKEMIA, MONOCYTIC, ACUTE; MALE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; PROGNOSIS;

EID: 2442604563     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2004.04921.x     Document Type: Article

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