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Volumn 16, Issue 6, 2000, Pages 1099-1105
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Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders.
a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
AGED;
ARTICLE;
BONE MARROW CELL;
CHROMOSOME DELETION;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETICS;
HUMAN;
KARYOTYPING;
MALE;
METHODOLOGY;
MIDDLE AGED;
MYELOPROLIFERATIVE DISORDER;
NUCLEIC ACID HYBRIDIZATION;
PATHOLOGY;
ADULT;
AGED;
BONE MARROW CELLS;
CHROMOSOME DELETION;
FEMALE;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
KARYOTYPING;
MALE;
MIDDLE AGED;
MYELOPROLIFERATIVE DISORDERS;
NUCLEIC ACID HYBRIDIZATION;
MLCS;
MLOWN;
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EID: 0034201384
PISSN: 10196439
EISSN: None
Source Type: Journal
DOI: 10.3892/ijo.16.6.1099 Document Type: Article |
Times cited : (16)
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References (0)
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