Translocation (X;20)(q13;q13.3): A nonrandom abnormality in four patients with myeloid disorders

Cancer Genetics and Cytogenetics

Volumn 157, Issue 1, 2005, Pages 70-73

  Reddy, Kavita S ^a   Richkind, Kathy ^a   Ross, Micheal ^b   Seirra, Rubin ^c  

^a GENZYME GENETICS   (United States)

^b Texas Cancer Care   (United States)

^c Columbia Basin Hematol Oncol PLLC ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ADULT; AGED; ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE PROBE; GENE REARRANGEMENT; GENE TRANSLOCATION; HUMAN; MALIGNANT TRANSFORMATION; MYELODYSPLASIA; MYELOFIBROSIS; MYELOID LEUKEMIA; PANCYTOPENIA; PRIORITY JOURNAL; SIDEROBLASTIC ANEMIA; THROMBOCYTOPENIA; X CHROMOSOME;

AGED; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, X; FEMALE; HUMANS; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; MYELOFIBROSIS; PANCYTOPENIA; TRANSLOCATION, GENETIC;

EID: 12844272839     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.05.014     Document Type: Article

References (6)

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6. B.A. Gray, D. Cornfield, A. Bent-Williams, and R.T. Zori Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders Cancer Genet Cytogenet 141 2003 169 174