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Showing results (31-40 of 89) with videos related to

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American Journal of Medical Genetics. Part A|September 16, 2004
Brachydactyly and short stature in a kindred with early-onset parkinsonismMarieke C J Dekker, R J H Galjaard, P J L M Snijders, et al.
American Journal of Human Genetics|April 3, 2001
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32J P Drenth, W H Finley, G J Breedveld, et al.
Genomics|January 1, 1993
Isolation and characterization of 25 unique DNA markers for human chromosome 22N A van Biezen, R H Lekanne Deprez, A Thijs, et al.
Molecular Psychiatry|June 28, 2006
The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohortsM F Gosso, E J C de Geus, M J van Belzen, et al.
Neurology|May 22, 2009
Familial aggregation of parkinsonism in progressive supranuclear palsyL Donker Kaat, A J W Boon, A Azmani, et al.
Neurology|June 1, 1997
Apolipoprotein E gene and sporadic frontal lobe dementiaM Stevens, C M van Duijn, P de Knijff, et al.
Brain : a Journal of Neurology|September 26, 2001
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22S M Rosso, W Kamphorst, B de Graaf, et al.
Brain : a Journal of Neurology|July 15, 2005
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathologyI F Bronner, B C ter Meulen, A Azmani, et al.
Annals of Neurology|November 30, 1999
FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutationA D Sperfeld, M B Collatz, H Baier, et al.
Molecular Psychiatry|August 9, 2006
Genetic and clinical analysis of a large Dutch Gilles de la Tourette familyA J M H Verkerk, D C Cath, H C van der Linde, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|September 16, 2004
Brachydactyly and short stature in a kindred with early-onset parkinsonismMarieke C J Dekker, R J H Galjaard, P J L M Snijders, et al.
American Journal of Human Genetics|April 3, 2001
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32J P Drenth, W H Finley, G J Breedveld, et al.
Genomics|January 1, 1993
Isolation and characterization of 25 unique DNA markers for human chromosome 22N A van Biezen, R H Lekanne Deprez, A Thijs, et al.
Molecular Psychiatry|June 28, 2006
The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohortsM F Gosso, E J C de Geus, M J van Belzen, et al.
Neurology|May 22, 2009
Familial aggregation of parkinsonism in progressive supranuclear palsyL Donker Kaat, A J W Boon, A Azmani, et al.
Neurology|June 1, 1997
Apolipoprotein E gene and sporadic frontal lobe dementiaM Stevens, C M van Duijn, P de Knijff, et al.
Brain : a Journal of Neurology|September 26, 2001
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22S M Rosso, W Kamphorst, B de Graaf, et al.
Brain : a Journal of Neurology|July 15, 2005
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathologyI F Bronner, B C ter Meulen, A Azmani, et al.
Annals of Neurology|November 30, 1999
FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutationA D Sperfeld, M B Collatz, H Baier, et al.
Molecular Psychiatry|August 9, 2006
Genetic and clinical analysis of a large Dutch Gilles de la Tourette familyA J M H Verkerk, D C Cath, H C van der Linde, et al.
Pageof 9