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Nederlands Tijdschrift Voor Geneeskunde|July 23, 1999
[Genes and genetics in Hirschsprung's disease]S M Maas, A S Brooks, R C Hennekam, et al.The British Journal of Surgery|May 3, 2000
Reduced endothelin-3 expression in sporadic Hirschsprung diseaseS E Kenny, R M Hofstra, C H Buys, et al.The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinomaR M Hofstra, O Fattoruso, L Quadro, et al.Prenatal Diagnosis|December 13, 2000
MASA syndrome: ultrasonographic evidence in a male fetusG Pomili, G Venti Donti, L Alunni Carrozza, et al.Nucleic Acids Research|November 25, 1998
Improvement of fragment and primer selection for mutation detection by denaturing gradient gel electrophoresisY Wu, V M Hayes, J Osinga, et al.The American Journal of Gastroenterology|October 29, 2000
Impact of KRAS and TP53 mutations on survival in patients with left- and right-sided Dukes' C colon cancerW A Bleeker, V M Hayes, A Karrenbeld, et al.Genes, Chromosomes & Cancer|November 7, 2000
New comprehensive denaturing-gradient-gel- electrophoresis assay for KRAS mutation detection applied to paraffin-embedded tumoursV M Hayes, J L Westra, E Verlind, et al.Journal of Pediatric Surgery|January 20, 1998
Coexistent Hirschsprung's disease and esophageal achalasia in male siblingsJ L Kelly, T M Mulcahy, D S O'Riordain, et al.Human Molecular Genetics|May 1, 1995
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung diseaseM Angrist, S Bolk, B Thiel, et al.Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locusS Bolk, A Pelet, R M Hofstra, et al.Pageof 6