Fluorescence in situ hybridization of progenitor cells obtained by fluorescence-activated cell sorting for the detection of cells affected by chromosome abnormality trisomy 8 in patients with myelodysplastic syndromes

Blood

Volumn 92, Issue 8, 1998, Pages 2886-2892

  Saitoh, Kohki ^a   Miura, Ikuo ^a   Takahashi, Naoto ^a   Miura, Akira B ^a  

^a AKITA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOLOGOUS BONE MARROW TRANSPLANTATION; CELL LINEAGE; CLINICAL ARTICLE; COLONY FORMING UNIT GEMM; FEMALE; FLUORESCENCE ACTIVATED CELL SORTER; FLUORESCENCE IN SITU HYBRIDIZATION; HEMATOPOIETIC STEM CELL; HUMAN; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; TRISOMY 8;

EID: 0032532037     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.8.2886.420k11_2886_2892     Document Type: Article

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