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Showing results (51-60 of 89) with videos related to

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European Journal of Human Genetics : EJHG|September 26, 2001
X-linked recessive inheritance of radial ray deficiencies in a family with four affected malesR J Galjaard, N Kostakoglu, J J Hoogeboom, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated familiesP Heutink, E M van Schothorst, A G van der Mey, et al.
American Journal of Human Genetics|November 25, 2000
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 geneP Ianakiev, van Baren MJ, M J Daly, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Human Genetics|February 1, 1991
Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genomeA J Pakstis, P Heutink, D L Pauls, et al.
Cell Death and Differentiation|August 15, 2009
Loss of function of DJ-1 triggered by Parkinson's disease-associated mutation is due to proteolytic resistance to caspase-6E Giaime, C Sunyach, C Druon, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
The Pharmacogenomics Journal|May 20, 2015
A common polymorphism in the ABCB1 gene is associated with side effects of PGP-dependent antidepressants in a large naturalistic Dutch cohortP M Bet, E C Verbeek, Y Milaneschi, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
European Journal of Human Genetics : EJHG|September 26, 2001
X-linked recessive inheritance of radial ray deficiencies in a family with four affected malesR J Galjaard, N Kostakoglu, J J Hoogeboom, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated familiesP Heutink, E M van Schothorst, A G van der Mey, et al.
American Journal of Human Genetics|November 25, 2000
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 geneP Ianakiev, van Baren MJ, M J Daly, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Human Genetics|February 1, 1991
Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genomeA J Pakstis, P Heutink, D L Pauls, et al.
Cell Death and Differentiation|August 15, 2009
Loss of function of DJ-1 triggered by Parkinson's disease-associated mutation is due to proteolytic resistance to caspase-6E Giaime, C Sunyach, C Druon, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
The Pharmacogenomics Journal|May 20, 2015
A common polymorphism in the ABCB1 gene is associated with side effects of PGP-dependent antidepressants in a large naturalistic Dutch cohortP M Bet, E C Verbeek, Y Milaneschi, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 9