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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 BuysNucleic 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.Chromosoma|January 1, 1980
Abundance of protein-bound sulfhydryl and disulfide groups at chromosomal nucleolus organizing regions: a cytochemical study on the selective silver staining of NORsC H Buys, J OsingaThe Histochemical Journal|September 1, 1981
The role of chromosomal proteins in the induction of a differential staining of sister chromatids by lightC H Buys, J OsingaChromosoma|January 1, 1984
Selective staining of the same set of nucleolar phosphoproteins by silver and Giemsa. A combined biochemical and cytochemical study on staining of NORsC H Buys, J OsingaNucleic 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.Human Genetics|January 1, 1981
Rapid irradiation procedure for obtaining permanent differential staining of sister chromatids and aspects of its underlying mechanismC H Buys, J Osinga, S StienstraMechanisms of Ageing and Development|August 1, 1979
Age-dependent variability of ribosomal RNA-gene activity in man as determined from frequencies of silver staining nucleolus organizing regions on metaphase chromosomes of lymphocytes and fibroblastsC H Buys, J Osinga, G J AndersNucleic Acids Research|September 25, 1999
Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresisV M Hayes, Y Wu, J Osinga, 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.Pageof 19