Transcription Mapping in a Medulloblastoma Breakpoint Interval and Smith–Magenis Syndrome Candidate Region: Identification of 53 Transcriptional Units and New Candidate Genes
- 15 February 1999
- Vol. 56 (1) , 1-11
- https://doi.org/10.1006/geno.1998.5647
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: Analysis of cell-cycle distribution and radiation sensitivityAmerican Journal of Medical Genetics, 1998
- Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndromeNature Genetics, 1997
- tom-1, a novel v-Myb target gene expressed in AMV- and E26-transformed myelomonocytic cellsThe EMBO Journal, 1997
- Definition of the critical interval for Smith-Magenis syndromeCytogenetic and Genome Research, 1997
- Grap Is a Novel SH3-SH2-SH3 Adaptor Protein That Couples Tyrosine Kinases to the Ras PathwayJournal of Biological Chemistry, 1996
- Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)American Journal of Medical Genetics, 1996
- Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneNature Genetics, 1996
- Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomasGenes, Chromosomes and Cancer, 1995
- Eye abnormalities in the Smith‐Magenis contiguous gene deletion syndromeAmerican Journal of Medical Genetics, 1993
- Structural chromosomal abnormalities in human medulloblastomaCancer Genetics and Cytogenetics, 1988