Single nucleotide polymorphism arrays complement metaphase cytogenetics in detection of new chromosomal lesions in MDS [11]

Leukemia

Volumn 21, Issue 9, 2007, Pages 2058-2061

  Gondek, L P ^a   Tiu, R ^a   Haddad, A S ^a   O'Keefe, C L ^a   Sekeres, M A ^a   Theil, K S ^b   Maciejewski, J P ^a  

^a TAUSSIG CANCER INSTITUTE   (United States)

^b LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; AGED; CHROMOSOME 1; CHROMOSOME 11Q; CHROMOSOME 13; CHROMOSOME 7Q; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME LOSS; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; CYTOGENETICS; GENE DELETION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HUMAN; KARYOTYPE 46,XY; LETTER; MAJOR CLINICAL STUDY; METAPHASE; MICROSATELLITE MARKER; MYELODYSPLASTIC SYNDROME; PATHOPHYSIOLOGY; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY 13; X CHROMOSOME;

EID: 34548125332     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/sj.leu.2404745     Document Type: Letter

References (8)

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