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M Alders

Showing results (21-30 of 44) with videos related to

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JIMD Reports|March 10, 2017
Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?M Fleger, J Willomitzer, R Meinsma, et al.
Circulation|September 24, 1999
Homozygous premature truncation of the HERG protein : the human HERG knockoutT Hoorntje, M Alders, P van Tintelen, et al.
European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 20, 2007
[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]N Hofman, P G Postema, I M van Langen, et al.
The Journal of Infectious Diseases|December 12, 2001
Adrenocorticotropic hormone and cortisol levels in relation to inflammatory response and disease severity in children with meningococcal diseaseJ B van Woensel, M H Biezeveld, A M Alders, et al.
Human Molecular Genetics|June 1, 1997
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsM Alders, M Hodges, A K Hadjantonakis, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|April 23, 2011
Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6P G Postema, I Christiaans, N Hofman, et al.
Journal of Medical Genetics|May 9, 2006
Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 geneR H Lekanne Deprez, J J Muurling-Vlietman, J Hruda, et al.
Genomics|June 1, 1994
An integrated physical map of 210 markers assigned to the short arm of human chromosome 11E Redeker, J M Hoovers, M Alders, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
JIMD Reports|March 10, 2017
Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?M Fleger, J Willomitzer, R Meinsma, et al.
Circulation|September 24, 1999
Homozygous premature truncation of the HERG protein : the human HERG knockoutT Hoorntje, M Alders, P van Tintelen, et al.
European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 20, 2007
[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]N Hofman, P G Postema, I M van Langen, et al.
The Journal of Infectious Diseases|December 12, 2001
Adrenocorticotropic hormone and cortisol levels in relation to inflammatory response and disease severity in children with meningococcal diseaseJ B van Woensel, M H Biezeveld, A M Alders, et al.
Human Molecular Genetics|June 1, 1997
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsM Alders, M Hodges, A K Hadjantonakis, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|April 23, 2011
Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6P G Postema, I Christiaans, N Hofman, et al.
Journal of Medical Genetics|May 9, 2006
Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 geneR H Lekanne Deprez, J J Muurling-Vlietman, J Hruda, et al.
Genomics|June 1, 1994
An integrated physical map of 210 markers assigned to the short arm of human chromosome 11E Redeker, J M Hoovers, M Alders, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Pageof 5