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Showing results (61-70 of 89) with videos related to

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American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
Neurology|June 20, 1998
Familial aggregation in frontotemporal dementiaM Stevens, C M van Duijn, W Kamphorst, et al.
American Journal of Human Genetics|February 11, 1999
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsP Rizzu, J C Van Swieten, M Joosse, et al.
Human Molecular Genetics|April 1, 1992
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qterP Heutink, A G van der Mey, L A Sandkuijl, et al.
Journal of Medical Genetics|February 9, 1999
Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36J Zguricas, H Heus, E Morales-Peralta, et al.
Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.
Journal of Neurology|September 25, 2003
A clinical-genetic study of Parkinson's disease in a genetically isolated communityM C J Dekker, J C van Swieten, J J Houwing-Duistermaat, et al.
Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
Neurology|June 20, 1998
Familial aggregation in frontotemporal dementiaM Stevens, C M van Duijn, W Kamphorst, et al.
American Journal of Human Genetics|February 11, 1999
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsP Rizzu, J C Van Swieten, M Joosse, et al.
Human Molecular Genetics|April 1, 1992
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qterP Heutink, A G van der Mey, L A Sandkuijl, et al.
Journal of Medical Genetics|February 9, 1999
Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36J Zguricas, H Heus, E Morales-Peralta, et al.
Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Clinical Genetics|February 27, 2013
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegiaC Bettencourt, J L López-Sendón, J García-Caldentey, et al.
Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.
Journal of Neurology|September 25, 2003
A clinical-genetic study of Parkinson's disease in a genetically isolated communityM C J Dekker, J C van Swieten, J J Houwing-Duistermaat, et al.
Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Pageof 9