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P Heutink

Showing results (41-50 of 89) with videos related to

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Nature Genetics|March 1, 1994
The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7qP Heutink, J Zguricas, L van Oosterhout, et al.
Annals of Neurology|October 8, 1999
Phenotypic variation in hereditary frontotemporal dementia with tau mutationsJ C van Swieten, M Stevens, S M Rosso, et al.
Neurology|December 3, 2008
Is olfactory impairment in Parkinson disease related to phenotypic or genotypic characteristics?D Verbaan, S Boesveldt, S M van Rooden, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Journal of Medical Genetics|July 1, 1990
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18P Heutink, B J van de Wetering, G J Breedveld, et al.
Annals of Neurology|February 1, 1997
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch familiesP Heutink, M Stevens, P Rizzu, et al.
Neuroscience Letters|January 7, 2000
Mutation screening of the tau gene in patients with early-onset Alzheimer's diseaseG Roks, B Dermaut, P Heutink, et al.
Diabetes|March 15, 2001
A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarctionN Vaessen, P Heutink, J A Janssen, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
Genes, Brain, and Behavior|July 6, 2012
Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25T S Rizzi, G Beunders, P Rizzu, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Nature Genetics|March 1, 1994
The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7qP Heutink, J Zguricas, L van Oosterhout, et al.
Annals of Neurology|October 8, 1999
Phenotypic variation in hereditary frontotemporal dementia with tau mutationsJ C van Swieten, M Stevens, S M Rosso, et al.
Neurology|December 3, 2008
Is olfactory impairment in Parkinson disease related to phenotypic or genotypic characteristics?D Verbaan, S Boesveldt, S M van Rooden, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonismV Bonifati, P Rizzu, F Squitieri, et al.
Journal of Medical Genetics|July 1, 1990
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18P Heutink, B J van de Wetering, G J Breedveld, et al.
Annals of Neurology|February 1, 1997
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch familiesP Heutink, M Stevens, P Rizzu, et al.
Neuroscience Letters|January 7, 2000
Mutation screening of the tau gene in patients with early-onset Alzheimer's diseaseG Roks, B Dermaut, P Heutink, et al.
Diabetes|March 15, 2001
A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarctionN Vaessen, P Heutink, J A Janssen, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
Genes, Brain, and Behavior|July 6, 2012
Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25T S Rizzi, G Beunders, P Rizzu, et al.
Pageof 9