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American Journal of Human Genetics|December 5, 1998
The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestryN A Ellis, S Ciocci, M Proytcheva, et al.Human Molecular Genetics|July 1, 1993
Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposisP Paul, T Letteboer, L Gelbert, et al.Research in Developmental Disabilities|January 1, 1987
Effects of fenfluramine on the behavior of autistic individualsG Groden, J Groden, M Dondey, et al.Genetic Testing|August 28, 1999
High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish originL Shahrabani-Gargir, R Shomrat, Y Yaron, et al.Human Mutation|March 3, 1998
A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome geneJ E Straughen, J Johnson, D McLaren, et al.Gastroenterology|August 7, 2001
Numerous colonic adenomas in an individual with Bloom's syndromeA M Lowy, J J Kordich, V Gismondi, et al.American Journal of Human Genetics|May 1, 1994
Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli regionL B Jorde, W S Watkins, M Carlson, et al.Cancer Research|December 1, 1993
A rapid screening method to detect nonsense and frameshift mutations: identification of disease-causing APC allelesL Varesco, J Groden, L Spirio, et al.Genes, Chromosomes & Cancer|July 1, 1997
Regenerative lesions in ulcerative colitis are characterized by microsatellite mutationC D Heinen, A E Noffsinger, J Belli, et al.The Journal of Biological Chemistry|April 28, 2001
The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repairG Langland, J Kordich, J Creaney, et al.Pageof 5