Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia

International Journal of Laboratory Hematology

Volumn 32, Issue 1 PART.1, 2010, Pages

  Xu, W ^a   Li, J Y ^a   Liu, Q ^a   Zhu, Y ^a   Pan, J L ^b   Qiu, H R ^a   Xue, Y Q ^b  

^a THE FIRST AFFILIATED HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

^b SOOCHOW UNIVERSITY   (China)

Author keywords

Acute myeloid leukemia; Complex chromosomal aberrations; Multiplex fluorescence in situ hybridization; Myelodysplastic syndromes

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; CHROMOSOME; CHROMOSOME 11; CHROMOSOME 17; CHROMOSOME 18; CHROMOSOME 19; CHROMOSOME 21; CHROMOSOME 6; CHROMOSOME 7; CHROMOSOME 8; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INCIDENCE; KARYOTYPE; MALE; MONOSOMY; MULTIPLEX FLUORESCENCE IN SITU HYBRIDIZATION; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; TRISOMY;

ADOLESCENT; ADULT; AGED; CHILD; CHROMOSOMES, HUMAN; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOID, ACUTE; MALE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; TRANSLOCATION, GENETIC; TRISOMY;

EID: 77249123492     PISSN: 17515521     EISSN: 1751553X     Source Type: Journal    
DOI: 10.1111/j.1751-553X.2008.01101.x     Document Type: Article

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