Spurious monosomy 7 in leukemia due to centromeric heteromorphism

Cancer Genetics and Cytogenetics

Volumn 119, Issue 1, 2000, Pages 67-69

  Duval, Alex ^a   Feneux, Danielle ^a   Sutton, Laurent ^b   Tchernia, Gil ^a   Léonard, Claude ^a  

^a Service d'Hématologie   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE MARROW CELL; CASE REPORT; CHROMOSOME 7; CYTOGENETICS; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LYMPHATIC LEUKEMIA; MONOSOMY 7; PRIORITY JOURNAL;

ADULT; BONE MARROW TRANSPLANTATION; CENTROMERE; CHROMOSOMES, HUMAN, PAIR 7; COMBINED MODALITY THERAPY; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, B-CELL, ACUTE; MONOSOMY;

POMACANTHUS MACULOSUS;

EID: 0034016474     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00204-6     Document Type: Article

References (4)

1. Kadam P., Umerani A., Srivastava A., Materson M., Lampkin B., Raza A. Combination of classical and interphase cytogenetics to investigate the biology of myeloid disorders. detection of masked monosomy 7 in AML Leuk Res. 17:1993;365-374.
2. Kadam P., Masterson M., Soukup S., Moore C., Raza A., Lampkin B.C. Detection of unexpected clones of monosomy 7 in childhood acute lymphoblastic leukemia using fluorescence in situ hybridization. Anticancer Res. 14:1994;545-548.
3. Lin M.S., Zhang A., Fujimoto A., Wilson M.G. A rare 6q11+ heteromorphism. cytogenetic analysis and in situ hybridization Hum Hered. 44:1994;31-36.
4. Bonfatti A., Giunta C., Sensi A., Gruppioni R., Rubbini M., Fontana F. Heteromorphism of human chromosome 18 detected by fluorescent in situ hybridization. Eur J Histochem. 37:1993;149-154.