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Genes, Chromosomes & Cancer|March 10, 1998
Pre-clinical evaluation of probes to detect t(8;21) AML minimal residual disease by fluorescence in situ hybridizationG A Paskulin, G Philips, R Morgan, et al.
American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
Oncogene|July 22, 1998
Analysis of TEL proteins in human leukemiasH Poirel, V Lacronique, M Mauchauffé, et al.
Cancer Research|January 1, 1997
Identification of a novel region of homozygous deletion on chromosome 9p in squamous cell carcinoma of the lung: the location of a putative tumor suppressor geneJ S Wiest, W A Franklin, J T Otstot, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
Nucleic Acids Research|December 19, 2003
The Gene Ontology (GO) database and informatics resourceM A Harris, J Clark, A Ireland, et al.
Nucleic Acids Research|November 20, 2012
Gene Ontology annotations and resources, J A Blake, M Dolan, et al.
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