der(1)t(1;19)(p12;p11): A new nonrandom chromosomal abnormality in myelodysplastic syndrome

Cancer Genetics and Cytogenetics

Volumn 94, Issue 2, 1997, Pages 85-87

  Gill, Javed Iqbal ^a   Varela, Maria ^a   Tsien, Fern ^a   Krause, John Richard ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE MARROW CELL; CASE REPORT; CHROMOSOME 1; CHROMOSOME 19; CHROMOSOME 20; CHROMOSOME 7; CHROMOSOME ABERRATION; CHROMOSOME DELETION 5; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; KARYOTYPE; MALE; MONOSOMY; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 19; HUMANS; MALE; MYELODYSPLASTIC SYNDROMES; TRANSLOCATION, GENETIC;

EID: 0030994036     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00188-4     Document Type: Article

References (10)

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