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Peter Heutink

Showing results (91-100 of 240) with videos related to

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American Journal of Medical Genetics. Part A|August 12, 2003
Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspringRobert-Jan H Galjaard, Herma C van der Linde, Bert H J Eussen, et al.
European Journal of Human Genetics : EJHG|April 1, 2004
Linkage disequilibrium in young genetically isolated Dutch populationYurii S Aulchenko, Peter Heutink, Ian Mackay, et al.
Annals of Neurology|September 22, 2015
Is the MC1R variant p.R160W associated with Parkinson's?Steven J Lubbe, Valentina Escott-Price, Alexis Brice, et al.
European Journal of Human Genetics : EJHG|May 8, 2003
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34Robert-Jan H Galjaard, Arie P T Smits, Joep H A M Tuerlings, et al.
Brain Communications|October 25, 2021
Evidence for <i>GRN</i> connecting multiple neurodegenerative diseasesMike A Nalls, Cornelis Blauwendraat, Lana Sargent, et al.
Annals of Neurology|January 6, 2004
DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementiaPatrizia Rizzu, David A Hinkle, Victoria Zhukareva, et al.
Diabetes|March 2, 2002
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the NetherlandsNorbert Vaessen, Peter Heutink, Jeanine J Houwing-Duistermaat, et al.
Life Science Alliance|February 23, 2021
Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosisArun Pal, Benedikt Kretner, Masin Abo-Rady, et al.
American Journal of Human Genetics|December 19, 2002
A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]John C van Swieten, Esther Brusse, Bianca M de Graaf, et al.
Molecular Neurobiology|January 6, 2019
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative DiseasesSilvia Zucchelli, Stefania Fedele, Paolo Vatta, et al.
Pageof 24

Showing results (91-100 of 240) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part A|August 12, 2003
Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspringRobert-Jan H Galjaard, Herma C van der Linde, Bert H J Eussen, et al.
European Journal of Human Genetics : EJHG|April 1, 2004
Linkage disequilibrium in young genetically isolated Dutch populationYurii S Aulchenko, Peter Heutink, Ian Mackay, et al.
Annals of Neurology|September 22, 2015
Is the MC1R variant p.R160W associated with Parkinson's?Steven J Lubbe, Valentina Escott-Price, Alexis Brice, et al.
European Journal of Human Genetics : EJHG|May 8, 2003
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34Robert-Jan H Galjaard, Arie P T Smits, Joep H A M Tuerlings, et al.
Brain Communications|October 25, 2021
Evidence for <i>GRN</i> connecting multiple neurodegenerative diseasesMike A Nalls, Cornelis Blauwendraat, Lana Sargent, et al.
Annals of Neurology|January 6, 2004
DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementiaPatrizia Rizzu, David A Hinkle, Victoria Zhukareva, et al.
Diabetes|March 2, 2002
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the NetherlandsNorbert Vaessen, Peter Heutink, Jeanine J Houwing-Duistermaat, et al.
Life Science Alliance|February 23, 2021
Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosisArun Pal, Benedikt Kretner, Masin Abo-Rady, et al.
American Journal of Human Genetics|December 19, 2002
A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]John C van Swieten, Esther Brusse, Bianca M de Graaf, et al.
Molecular Neurobiology|January 6, 2019
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative DiseasesSilvia Zucchelli, Stefania Fedele, Paolo Vatta, et al.
Pageof 24