Analysis of loss of heterozygosity at 16p12-p13 (familial neuroblastoma locus) in 470 neuroblastomas including both sporadic and mass screening tumors
- 30 November 2000
- journal article
- research article
- Published by Wiley in Medical and Pediatric Oncology
- Vol. 35 (6) , 531-533
- https://doi.org/10.1002/1096-911x(20001201)35:6<531::aid-mpo6>3.0.co;2-2
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Localization of a Target Region of Allelic Loss to a 1-cM Interval on Chromosome 16p.13.13 in Hepatocellular CarcinomaJapanese Journal of Cancer Research, 1999
- Absence of mutation of the p73 gene localized at chromosome 1p36.3 in hepatocellular carcinomaBritish Journal of Cancer, 1998
- A model for p53-induced apoptosisNature, 1997
- Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair EndonucleaseCell, 1996
- Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridizationCytogenetic and Genome Research, 1996
- Loss of heterozygosity on chromosome arms 5q, IIp, IIq, I3q, and I6p in Human Testicular Germ Cell TumorsGenes, Chromosomes and Cancer, 1995
- Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patientsNature Genetics, 1994
- Association between High Levels of Expression of the TRK Gene and Favorable Outcome in Human NeuroblastomaNew England Journal of Medicine, 1993
- Mapping of the humanGSPT1 gene, a human homolog of the yeastGST1 gene, to chromosomal band 16p13.1Somatic Cell and Molecular Genetics, 1992
- Familial neuroblastoma. Case reports, literature review, and etiologic considerationsCancer, 1986