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Comparative genomic hybridization study of primary neuroblastoma tumors
Author(s): Lastowska M, Nacheva E, McGuckin A, Curtis A, Grace C, Pearson A, Bown N
Source: GENES CHROMOSOMES & CANCER    Volume: 18    Issue: 3    Pages: 162-169    Published: MAR 1997  
Times Cited: 78     References: 30     
Abstract: Neuroblastoma tumors show a complex interaction of genetic abnormalities, among which some are of significant prognostic importance; however, analysis of chromosome changes in this tumor is often unsuccessful. Twenty primary tumors were studied by comparative genomic hybridization (CGH), and abnormalities were found in 19. While these changes included deletions of chromosome arm 1p (45%) and MYCN oncogene amplification (30%), gains of chromosome 17 material were much more frequent (75%). We also found evidence in two cases of a new amplification site at band 2p23. (C) 1997 Wiley-Liss, Inc.
Document Type: Article
Language: English
Reprint Address: Lastowska, M (reprint author), UNIV NEWCASTLE, DEPT HUMAN GENET, 19-20 CLAREMONT PL, NEWCASTLE UPON TYNE NE2 4AA, TYNE & WEAR ENGLAND
Addresses:
1. UNIV NEWCASTLE, DEPT CHILD HLTH, NEWCASTLE UPON TYNE NE2 4AA, TYNE & WEAR ENGLAND
2. UNIV NEWCASTLE, CANC RES UNIT, NEWCASTLE UPON TYNE NE2 4AA, TYNE & WEAR ENGLAND
3. UNIV CAMBRIDGE, ADDENBROOKES HOSP, DEPT HAEMATOL, CAMBRIDGE CB2 1TN, ENGLAND
4. ROYAL VICTORIA INFIRM, DEPT PATHOL, NEWCASTLE UPON TYNE NE1 4LP, TYNE & WEAR ENGLAND
5. DIGITAL SCI LTD, CAMBRIDGE, ENGLAND
6. INST PAEDIAT, CLIN PAEDIAT HAEMATOL & ONCOL, POZNAN, POLAND
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC, 605 THIRD AVE, NEW YORK, NY 10158-0012
Subject Category: Oncology; Genetics & Heredity
IDS Number: WM741
ISSN: 1045-2257
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