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C Hamel

Showing results (201-210 of 291) with videos related to

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European Journal of Medical Genetics|December 9, 2008
Compound-heterozygous Marfan syndromeF S Van Dijk, B C Hamel, Y Hilhorst-Hofstee, et al.
Clinical Genetics|August 26, 1998
Ehlers-Danlos syndrome and type III collagen abnormalities: a variable clinical spectrumB C Hamel, G Pals, C H Engels, et al.
American Journal of Medical Genetics. Part A|March 13, 2012
Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutationN C Voermans, M Kempers, M Lammens, et al.
American Journal of Medical Genetics|December 1, 1992
False-negative prenatal diagnosis of restrictive dermopathyB C Hamel, R Happle, P M Steylen, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|December 25, 2008
Risk factors associated with recent transmission of tuberculosis: systematic review and meta-analysisE Nava-Aguilera, N Andersson, E Harris, et al.
Journal Des Maladies Vasculaires|January 1, 1989
[The history of Horton's disease or ... 10 centuries of a fascinating adventure]J P Henriet, J Marin, J Gosselin, et al.
Zoological Science|June 1, 1995
Neuroendocrine communication in the frog adrenal glandO Lesouhaitier, M Esneu, M K Kodjo, et al.
Mitochondrion|August 27, 2005
Quantification of total mitochondrial DNA and the 4977-bp common deletion in Pearson's syndrome lymphoblasts using a fluorogenic 5'-nuclease (TaqMan) real-time polymerase chain reaction assay and plasmid external calibration standardsWendy Knapp Pogozelski, Christine J C Hamel, Collynn F Woeller, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Pageof 30

Showing results (201-210 of 291) with videos related to

Sort By:
Pageof 30
European Journal of Medical Genetics|December 9, 2008
Compound-heterozygous Marfan syndromeF S Van Dijk, B C Hamel, Y Hilhorst-Hofstee, et al.
Clinical Genetics|August 26, 1998
Ehlers-Danlos syndrome and type III collagen abnormalities: a variable clinical spectrumB C Hamel, G Pals, C H Engels, et al.
American Journal of Medical Genetics. Part A|March 13, 2012
Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutationN C Voermans, M Kempers, M Lammens, et al.
American Journal of Medical Genetics|December 1, 1992
False-negative prenatal diagnosis of restrictive dermopathyB C Hamel, R Happle, P M Steylen, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|December 25, 2008
Risk factors associated with recent transmission of tuberculosis: systematic review and meta-analysisE Nava-Aguilera, N Andersson, E Harris, et al.
Journal Des Maladies Vasculaires|January 1, 1989
[The history of Horton's disease or ... 10 centuries of a fascinating adventure]J P Henriet, J Marin, J Gosselin, et al.
Zoological Science|June 1, 1995
Neuroendocrine communication in the frog adrenal glandO Lesouhaitier, M Esneu, M K Kodjo, et al.
Mitochondrion|August 27, 2005
Quantification of total mitochondrial DNA and the 4977-bp common deletion in Pearson's syndrome lymphoblasts using a fluorogenic 5'-nuclease (TaqMan) real-time polymerase chain reaction assay and plasmid external calibration standardsWendy Knapp Pogozelski, Christine J C Hamel, Collynn F Woeller, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Helvetica Paediatrica Acta|February 1, 1978
Oculocutaneous albinism associated with motor neuron diseaseB C Hamel, R C Sengers, A M Stadhouders, et al.
Pageof 30