Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes

Blood

Volumn 87, Issue 4, 1996, Pages 1561-1570

  Asimakopoulos, Fotios A ^b   Holloway, Tracey L ^b   Nacheva, Elisabeth P ^b   Scott, Michael A ^b   Fenaux, Pierre ^b   Green, Anthony R ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; APLASTIC ANEMIA; ARTICLE; CHROMOSOME 20Q; CHROMOSOME DELETION; CHROMOSOME G BAND; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GRANULOCYTE; GRANULOPOIESIS; HUMAN; HUMAN CELL; MALE; MYELODYSPLASTIC SYNDROME; MYELOPROLIFERATIVE DISORDER; PERIPHERAL CIRCULATION; POLYCYTHEMIA VERA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SIDEROBLASTIC ANEMIA;

EID: 0030043357     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v87.4.1561.bloodjournal8741561     Document Type: Article

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