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Showing results (21-30 of 89) with videos related to

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Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|July 9, 2002
[Radiologische Besonderheiten einer bilateral vererblichen Mikro-Epiphysendysplasie - deutliche Entität einer Skelettdysplasie]A K Mostert, P F Dijkstra, J R Van Horn, et al.
Handchirurgie, Mikrochirurgie, Plastische Chirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse : Organ Der V|July 1, 1996
Genetic aspects of polydactylyJ Zguricas, P Heutink, L Heredero, et al.
Neurology|May 12, 2004
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephalyU Aguglia, A Gambardella, G J Breedveld, et al.
Genes, Brain, and Behavior|October 3, 2007
Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohortsM F Gosso, E J C de Geus, T J C Polderman, et al.
American Journal of Human Genetics|August 1, 1995
Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?P Heutink, B J van de Wetering, A J Pakstis, et al.
Genes, Brain, and Behavior|November 4, 2006
Association between the CHRM2 gene and intelligence in a sample of 304 Dutch familiesM F Gosso, M van Belzen, E J C de Geus, et al.
Neurology|November 26, 2003
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonismP Ibáñez, G De Michele, V Bonifati, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
Journal of Medical Genetics|December 1, 1994
Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneityP Heutink, T Haitjema, G J Breedveld, et al.
International Orthopaedics|June 20, 2002
Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-upA K Mostert, B R H Jansen, P F Dijkstra, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|July 9, 2002
[Radiologische Besonderheiten einer bilateral vererblichen Mikro-Epiphysendysplasie - deutliche Entität einer Skelettdysplasie]A K Mostert, P F Dijkstra, J R Van Horn, et al.
Handchirurgie, Mikrochirurgie, Plastische Chirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse : Organ Der V|July 1, 1996
Genetic aspects of polydactylyJ Zguricas, P Heutink, L Heredero, et al.
Neurology|May 12, 2004
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephalyU Aguglia, A Gambardella, G J Breedveld, et al.
Genes, Brain, and Behavior|October 3, 2007
Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohortsM F Gosso, E J C de Geus, T J C Polderman, et al.
American Journal of Human Genetics|August 1, 1995
Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?P Heutink, B J van de Wetering, A J Pakstis, et al.
Genes, Brain, and Behavior|November 4, 2006
Association between the CHRM2 gene and intelligence in a sample of 304 Dutch familiesM F Gosso, M van Belzen, E J C de Geus, et al.
Neurology|November 26, 2003
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonismP Ibáñez, G De Michele, V Bonifati, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
Journal of Medical Genetics|December 1, 1994
Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneityP Heutink, T Haitjema, G J Breedveld, et al.
International Orthopaedics|June 20, 2002
Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-upA K Mostert, B R H Jansen, P F Dijkstra, et al.
Pageof 9