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M E Lewis

Showing results (141-150 of 153) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Correction of hypertriglyceridemia and impaired fat tolerance in lipoprotein lipase-deficient mice by adenovirus-mediated expression of human lipoprotein lipaseK J Excoffon, G Liu, L Miao, et al.
Chronic Diseases and Injuries in Canada|March 15, 2012
Correlates of age at diagnosis of autism spectrum disorders in six Canadian regionsH Coo, H Ouellette-Kuntz, M Lam, et al.
Journal of Medical Genetics|February 23, 2023
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG)Melissa T Carter, Myriam Srour, Ping-Yee Billie Au, et al.
Clinical Genetics|February 29, 2012
Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disabilityY Qiao, C Tyson, M Hrynchak, et al.
European Journal of Clinical Investigation|March 27, 1999
Lipid and lipoprotein analysis of cats with lipoprotein lipase deficiencyD G Ginzinger, S M Clee, J Dallongeville, et al.
The Journal of Thoracic and Cardiovascular Surgery|December 14, 1999
Replacement of the proximal aorta and aortic valve using a composite bileaflet prosthesis and gelatin-impregnated polyester graft (Carbo-Seal): early results in 143 patientsS M Langley, S J Rooney, M J Dalrymple-Hay, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Orphanet Journal of Rare Diseases|August 10, 2011
Understanding the impact of 1q21.1 copy number variantChansonette Harvard, Emma Strong, Eloi Mercier, et al.
Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Pageof 16

Showing results (141-150 of 153) with videos related to

Sort By:
Pageof 16
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Correction of hypertriglyceridemia and impaired fat tolerance in lipoprotein lipase-deficient mice by adenovirus-mediated expression of human lipoprotein lipaseK J Excoffon, G Liu, L Miao, et al.
Chronic Diseases and Injuries in Canada|March 15, 2012
Correlates of age at diagnosis of autism spectrum disorders in six Canadian regionsH Coo, H Ouellette-Kuntz, M Lam, et al.
Journal of Medical Genetics|February 23, 2023
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG)Melissa T Carter, Myriam Srour, Ping-Yee Billie Au, et al.
Clinical Genetics|February 29, 2012
Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disabilityY Qiao, C Tyson, M Hrynchak, et al.
European Journal of Clinical Investigation|March 27, 1999
Lipid and lipoprotein analysis of cats with lipoprotein lipase deficiencyD G Ginzinger, S M Clee, J Dallongeville, et al.
The Journal of Thoracic and Cardiovascular Surgery|December 14, 1999
Replacement of the proximal aorta and aortic valve using a composite bileaflet prosthesis and gelatin-impregnated polyester graft (Carbo-Seal): early results in 143 patientsS M Langley, S J Rooney, M J Dalrymple-Hay, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Orphanet Journal of Rare Diseases|August 10, 2011
Understanding the impact of 1q21.1 copy number variantChansonette Harvard, Emma Strong, Eloi Mercier, et al.
Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Pageof 16