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H K van Amstel

Showing results (1-10 of 11) with videos related to

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Nucleic Acids Research|August 25, 1990
Tetranucleotide repeat polymorphism in the vWF geneH K van Amstel, P H Reitsma
Journal of the National Cancer Institute|October 19, 2000
Mutational analysis of endothelial cells derived from von Hippel-Lindau-related renal cancerM Los, O A Kerckhaert, R Zewald, et al.
Nature Genetics|March 31, 2000
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humansM J van den Boogaard, M Dorland, F A Beemer, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
Molecular basis of hereditary protein C and protein S deficiencyP H Reitsma, H K van Amstel, B R Poort, et al.
American Journal of Human Genetics|June 13, 1998
Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphroditeJ C Giltay, T Brunt, F A Beemer, et al.
Journal of Pediatric Surgery|May 11, 1999
Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young childrenL W van Heurn, C Schaap, G Sie, et al.
Nature|January 27, 1994
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinomaR M Hofstra, R M Landsvater, I Ceccherini, et al.
American Journal of Human Genetics|February 1, 1995
X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunitI E van den Berg, E A van Beurden, H E Malingré, et al.
Archives of Neurology|November 16, 2001
Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch familiesR J Sinke, E F Ippel, C M Diepstraten, et al.
The American Journal of Medicine|December 1, 1996
Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large familyA M Moers, R M Landsvater, C Schaap, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|August 25, 1990
Tetranucleotide repeat polymorphism in the vWF geneH K van Amstel, P H Reitsma
Journal of the National Cancer Institute|October 19, 2000
Mutational analysis of endothelial cells derived from von Hippel-Lindau-related renal cancerM Los, O A Kerckhaert, R Zewald, et al.
Nature Genetics|March 31, 2000
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humansM J van den Boogaard, M Dorland, F A Beemer, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
Molecular basis of hereditary protein C and protein S deficiencyP H Reitsma, H K van Amstel, B R Poort, et al.
American Journal of Human Genetics|June 13, 1998
Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphroditeJ C Giltay, T Brunt, F A Beemer, et al.
Journal of Pediatric Surgery|May 11, 1999
Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young childrenL W van Heurn, C Schaap, G Sie, et al.
Nature|January 27, 1994
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinomaR M Hofstra, R M Landsvater, I Ceccherini, et al.
American Journal of Human Genetics|February 1, 1995
X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunitI E van den Berg, E A van Beurden, H E Malingré, et al.
Archives of Neurology|November 16, 2001
Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch familiesR J Sinke, E F Ippel, C M Diepstraten, et al.
The American Journal of Medicine|December 1, 1996
Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large familyA M Moers, R M Landsvater, C Schaap, et al.
Pageof 2