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Showing results (121-130 of 140) with videos related to

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European Journal of Sport Science|July 12, 2025
Tackle Height and Tackle Success-An Analysis of 52,204 Tackle EventsS Hendricks, K Till, S Scantlebury, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13Ratna N G B Tan, Ruben S G M Witlox, Yvonne Hilhorst-Hofstee, et al.
Journal of Medical Genetics|August 30, 2008
Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patientsC Zweier, H Sticht, E K Bijlsma, et al.
Journal of Medical Genetics|October 23, 2009
Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysisYvonne J Vos, Hermien E K de Walle, Krista K Bos, et al.
Nature Genetics|March 20, 2012
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeGijs W E Santen, Emmelien Aten, Yu Sun, et al.
JAMA|December 9, 2020
Effect of a Lower vs Higher Positive End-Expiratory Pressure Strategy on Ventilator-Free Days in ICU Patients Without ARDS: A Randomized Clinical Trial, Anna Geke Algera, Luigi Pisani, et al.
European Journal of Human Genetics : EJHG|June 25, 2009
CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysisFleur S Van Dijk, Isabel M Nesbitt, Peter G J Nikkels, et al.
Clinical Genetics|August 2, 2011
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1BC Halgren, S Kjaergaard, M Bak, et al.
European Heart Journal Open|March 27, 2023
Hyperlipidaemia elicits an atypical, T helper 1-like CD4<sup>+</sup> T-cell response: a key role for very low-density lipoproteinBram W van Os, Winnie G Vos, Laura A Bosmans, et al.
American Journal of Medical Genetics. Part A|October 1, 2015
Recurrent duplications of 17q12 associated with variable phenotypesElyse Mitchell, Andrew Douglas, Susanne Kjaegaard, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
European Journal of Sport Science|July 12, 2025
Tackle Height and Tackle Success-An Analysis of 52,204 Tackle EventsS Hendricks, K Till, S Scantlebury, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13Ratna N G B Tan, Ruben S G M Witlox, Yvonne Hilhorst-Hofstee, et al.
Journal of Medical Genetics|August 30, 2008
Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patientsC Zweier, H Sticht, E K Bijlsma, et al.
Journal of Medical Genetics|October 23, 2009
Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysisYvonne J Vos, Hermien E K de Walle, Krista K Bos, et al.
Nature Genetics|March 20, 2012
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeGijs W E Santen, Emmelien Aten, Yu Sun, et al.
JAMA|December 9, 2020
Effect of a Lower vs Higher Positive End-Expiratory Pressure Strategy on Ventilator-Free Days in ICU Patients Without ARDS: A Randomized Clinical Trial, Anna Geke Algera, Luigi Pisani, et al.
European Journal of Human Genetics : EJHG|June 25, 2009
CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysisFleur S Van Dijk, Isabel M Nesbitt, Peter G J Nikkels, et al.
Clinical Genetics|August 2, 2011
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1BC Halgren, S Kjaergaard, M Bak, et al.
European Heart Journal Open|March 27, 2023
Hyperlipidaemia elicits an atypical, T helper 1-like CD4<sup>+</sup> T-cell response: a key role for very low-density lipoproteinBram W van Os, Winnie G Vos, Laura A Bosmans, et al.
American Journal of Medical Genetics. Part A|October 1, 2015
Recurrent duplications of 17q12 associated with variable phenotypesElyse Mitchell, Andrew Douglas, Susanne Kjaegaard, et al.
Pageof 14