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H J Smeets

Showing results (11-20 of 57) with videos related to

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Genomics|February 1, 1991
Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locusH J Smeets, R Hermens, H G Brunner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 20, 1999
The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex IR F de Coo, P A Buddiger, H J Smeets, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 1, 1996
Identification of post-transplant anti-alpha 5 (IV) collagen alloantibodies in X-linked Alport syndromeP Dehan, L P Van den Heuvel, H J Smeets, et al.
Journal of Lipid Research|September 1, 1988
Identification of apolipoprotein E polymorphism by using synthetic oligonucleotidesH J Smeets, J Poddighe, P M Stuyt, et al.
American Journal of Medical Genetics|September 1, 1994
Familial Angelman syndrome with a crossover in the critical deletion regionM R Nelen, C J Van der Burgt, W N Nillesen, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Acta Chirurgica Belgica|May 31, 2011
Outcome of patients with ruptured abdominal aortic aneurysm after cardiopulmonary resuscitationA P A Greeven, L H Bouwman, H J Smeets, et al.
Journal of Medical Genetics|April 3, 2007
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation diseaseM J Blok, L Spruijt, I F M de Coo, et al.
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Genomics|February 1, 1991
Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locusH J Smeets, R Hermens, H G Brunner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 20, 1999
The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex IR F de Coo, P A Buddiger, H J Smeets, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 1, 1996
Identification of post-transplant anti-alpha 5 (IV) collagen alloantibodies in X-linked Alport syndromeP Dehan, L P Van den Heuvel, H J Smeets, et al.
Journal of Lipid Research|September 1, 1988
Identification of apolipoprotein E polymorphism by using synthetic oligonucleotidesH J Smeets, J Poddighe, P M Stuyt, et al.
American Journal of Medical Genetics|September 1, 1994
Familial Angelman syndrome with a crossover in the critical deletion regionM R Nelen, C J Van der Burgt, W N Nillesen, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Acta Chirurgica Belgica|May 31, 2011
Outcome of patients with ruptured abdominal aortic aneurysm after cardiopulmonary resuscitationA P A Greeven, L H Bouwman, H J Smeets, et al.
Journal of Medical Genetics|April 3, 2007
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation diseaseM J Blok, L Spruijt, I F M de Coo, et al.
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Pageof 6