19p Deletion in recurring leiomyosarcoma lesions from the same patient

Cancer Genetics and Cytogenetics

Volumn 119, Issue 2, 2000, Pages 102-108

  Riva, Paola ^a   Dalprà, Leda ^a   Gualandri, Valter ^a   Volontè, Marinella ^a   Miozzo, Monica ^a   Malgara, Roberta ^a   Conti, Annamaria Fuhrman ^a   Larizza, Lidia ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 19P; CHROMOSOME 22; CHROMOSOME ABERRATION; CONTROLLED STUDY; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HISTOLOGY; HUMAN; LEIOMYOSARCOMA; METHODOLOGY; MICROSATELLITE INSTABILITY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECURRENT CANCER;

ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 19; HUMANS; IN SITU HYBRIDIZATION; KARYOTYPING; LEIOMYOSARCOMA; MALE; MICROSATELLITE REPEATS; NEOPLASM PROTEINS; NEOPLASM RECURRENCE, LOCAL; NEOPLASMS, SECOND PRIMARY; SOFT TISSUE NEOPLASMS; TUMOR MARKERS, BIOLOGICAL;

EID: 0034080606     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00222-8     Document Type: Article

References (14)

1. Sreekantaiah C., Davis J.R., Sandberg A.A. Chromosomal abnormalities in leiomyosarcoma. Am J Pathol. 32:1993;263-266.
2. Sreekantaiah C., Ladanyl E.R., Chaganti R.S.K. Chromosomal aberrations in soft tissue tumors. Am J Pathol. 144:1994;1121-1134.
3. Schneider B.F., Lovell M.A., Golden W.L. Cytogenetic abnormalities in primary bronchopulmonary leiomyosarcoma of childhood. Cancer Genet Cytogenet. 105:1998;145-151.
4. El-Rifai W., Sarlomo-Rikala M., Knuutila S., Miettinen M. DNA copy number changes in development and progression in leiomyosarcoma. Am J Pathol. 152:1998;985-990.
5. Swanson P.E., Wick M.R., Dehner L.P. Leiomyosarcoma of somatic soft tissues in childhood. an immunohistochemical analysis of six cases with ultra structural correlation Hum Pathol. 22:1991;569-577.
6. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.
7. Chumakov I.M., Rigault P., Le Gall I., Bellanne-Chantelot C., Billault A., Guillou S., Soularue P., Guasconi G., Poullier E., Gros I. A YAC contig map of the human genome. Nature. 377:1995;175-297.
8. Breen M., Arveiler B., Murray I., Gosden J.R., Porteus D. YAC mapping by FISH using Alu-PCR-generated probes. Genomics. 13:1992;726-730.
9. Riva P., Castorina P., Manoukian S., Dalprà L., Doneda L., Marini G., den Dunnen J., Larizza L. Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome. Hum Genet. 98:1996;646-650.
10. Gyapay G., Morissette J., Vignal A., Dib C., Fizames C., Millasseau P., Marc S., Bernardi G., Lathrop M., Weissenbach J. The 1993-94 Genethon human genetic linkage map. Nature Genet. 7:1994;246-339.
11. Mutirangura A., Kuwano A., Ledbetter S.A., Chinault A.C., Ledbetter D.H. Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15. Hum Mol Genet. 1:1992;139.
12. Mark J., Wedell B., Dahlenfors R., Havol G. Cytogenetic observations in a human gastric leiomyosarcoma. Cancer Genet Cytogenet. 37:1989;215-220.
13. Boghosian L., Dal Cin P., Turc-Carel C., Rao U., Karakousis C., Sait S.J., Sandberg A.A. Three possible cytogenetic subgroups of leiomyosarcoma. Cancer Genet Cytogenet. 43:1989;39-49.
14. Bardi G., Johansson B., Pandis N., Heom S., Madhal N., Bak-Jansen E., Fredricksen H., Andrén-Sandberg A., Mitelman F. Recurrent chromosome aberrations in abdominal smooth muscle tumors. Cancer Genet Cytogenet. 62:1992;43-46.