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H Scheffer

Showing results (71-80 of 154) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entityB M van der Sluijs, H J ter Laak, H Scheffer, et al.
Human Molecular Genetics|June 1, 1996
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 geneN J Van Orsouw, D Li, P van der Vlies, et al.
Zeitschrift Fur Gastroenterologie|May 13, 2015
[Economic burden of Clostridium difficile enterocolitis in German hospitals based on routine DRG data]R F Grube, W Heinlein, H Scheffer, et al.
Lancet (London, England)|January 13, 1996
Association between angiotensin-converting-enzyme gene polymorphism and failure of renoprotective therapyG G van Essen, P L Rensma, D de Zeeuw, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibriumH Scheffer, D J Bruinvels, G J te Meerman, et al.
Magnetic Resonance in Medicine|April 27, 2001
Detection of myocardial viability based on measurement of sodium content: A (23)Na-NMR studyM Horn, C Weidensteiner, H Scheffer, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervalsR F Kooy, E Verlind, R H Houwen, et al.
Neuromuscular Disorders : NMD|May 2, 2016
No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndromeJ van Vliet, A Verrips, A A Tieleman, et al.
Cancer Genetics and Cytogenetics|July 1, 1988
A human glioblastoma line with karyotypic nullisomy 13 containing several chromosome 13-specific sequencesK D Zang, H Fischer, A van der Hout, et al.
The Pharmacogenomics Journal|October 4, 2006
The association between HTR2C polymorphisms and obesity in psychiatric patients using antipsychotics: a cross-sectional studyH Mulder, B Franke, A Aart van der-Beek van der, et al.
Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:
Pageof 16
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entityB M van der Sluijs, H J ter Laak, H Scheffer, et al.
Human Molecular Genetics|June 1, 1996
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 geneN J Van Orsouw, D Li, P van der Vlies, et al.
Zeitschrift Fur Gastroenterologie|May 13, 2015
[Economic burden of Clostridium difficile enterocolitis in German hospitals based on routine DRG data]R F Grube, W Heinlein, H Scheffer, et al.
Lancet (London, England)|January 13, 1996
Association between angiotensin-converting-enzyme gene polymorphism and failure of renoprotective therapyG G van Essen, P L Rensma, D de Zeeuw, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibriumH Scheffer, D J Bruinvels, G J te Meerman, et al.
Magnetic Resonance in Medicine|April 27, 2001
Detection of myocardial viability based on measurement of sodium content: A (23)Na-NMR studyM Horn, C Weidensteiner, H Scheffer, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervalsR F Kooy, E Verlind, R H Houwen, et al.
Neuromuscular Disorders : NMD|May 2, 2016
No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndromeJ van Vliet, A Verrips, A A Tieleman, et al.
Cancer Genetics and Cytogenetics|July 1, 1988
A human glioblastoma line with karyotypic nullisomy 13 containing several chromosome 13-specific sequencesK D Zang, H Fischer, A van der Hout, et al.
The Pharmacogenomics Journal|October 4, 2006
The association between HTR2C polymorphisms and obesity in psychiatric patients using antipsychotics: a cross-sectional studyH Mulder, B Franke, A Aart van der-Beek van der, et al.
Pageof 16