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European Journal of Human Genetics : EJHG|July 1, 1997
Mutations in Hirschsprung disease: when does a mutation contribute to the phenotypeR M Hofstra, J Osinga, C H Buys
Nucleic Acids Research|August 24, 1999
Improved mutation detection in GC-rich DNA fragments by combined DGGE and CDGEY Wu, R P Stulp, P Elfferich, et al.
Journal of Medical Genetics|June 30, 2000
A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)A S Brooks, M H Breuning, J Osinga, et al.
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