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Genetic Counseling (Geneva, Switzerland)|May 3, 2001
Phenotypic variability of Cat-Eye syndromeM J Berends, G Tan-Sindhunata, B Leegte, et al.
American Journal of Medical Genetics|May 8, 2000
Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotypeG Tan-Sindhunata, S Castedo, B Leegte, et al.
Nature Genetics|April 1, 1996
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)R M Hofstra, J Osinga, G Tan-Sindhunata, et al.
Gut|November 21, 1998
Oncological implications of RET gene mutations in Hirschsprung's diseaseR H Sijmons, R M Hofstra, F A Wijburg, et al.
Circulation Research|December 11, 1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromesC Bezzina, M W Veldkamp, M P van Den Berg, et al.
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