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G Weber

Showing results (1161-1170 of 1,377) with videos related to

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Epilepsia|May 18, 2004
Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 familiesYvonne G Weber, Andrea Berger, Nerses Bebek, et al.
Human Genetics|September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2Anne Christians, Esra Kesdiren, Imke Hennies, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Journal of Intellectual Disability Research : JIDR|September 10, 2010
The P15 - a multinational assessment battery for collecting data on health indicators relevant to adults with intellectual disabilitiesJ Perry, C Linehan, M Kerr, et al.
Neurology. Genetics|December 28, 2018
Development of a rapid functional assay that predicts GLUT1 disease severitySasha M Zaman, Saul A Mullen, Slavé Petrovski, et al.
Vaccine|November 26, 2008
Eczema vaccinatum resulting from the transmission of vaccinia virus from a smallpox vaccinee: an investigation of potential fomites in the home environmentEdith Lederman, Roque Miramontes, John Openshaw, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 2001
Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclassesA Bhattacharjee, W G Richards, J Staunton, et al.
Italian Journal of Pediatrics|June 2, 2019
X-linked hypophosphatemic rickets: an Italian experts' opinion surveyF Emma, M Cappa, F Antoniazzi, et al.
Physical Review Letters|April 7, 2010
Spectral shape of the two-photon decay of the 2 1S0 state in he-like tinS Trotsenko, A Kumar, A V Volotka, et al.
Ecology and Evolution|April 24, 2025
Mite Domatia and Associated Mite Density in a North American Eastern Deciduous Forest in MichiganCarolyn D K Graham, Lillian R Bailey, Ashley E Cole, et al.
Pageof 138

Showing results (1161-1170 of 1,377) with videos related to

Sort By:
Pageof 138
Epilepsia|May 18, 2004
Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 familiesYvonne G Weber, Andrea Berger, Nerses Bebek, et al.
Human Genetics|September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2Anne Christians, Esra Kesdiren, Imke Hennies, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Journal of Intellectual Disability Research : JIDR|September 10, 2010
The P15 - a multinational assessment battery for collecting data on health indicators relevant to adults with intellectual disabilitiesJ Perry, C Linehan, M Kerr, et al.
Neurology. Genetics|December 28, 2018
Development of a rapid functional assay that predicts GLUT1 disease severitySasha M Zaman, Saul A Mullen, Slavé Petrovski, et al.
Vaccine|November 26, 2008
Eczema vaccinatum resulting from the transmission of vaccinia virus from a smallpox vaccinee: an investigation of potential fomites in the home environmentEdith Lederman, Roque Miramontes, John Openshaw, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 2001
Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclassesA Bhattacharjee, W G Richards, J Staunton, et al.
Italian Journal of Pediatrics|June 2, 2019
X-linked hypophosphatemic rickets: an Italian experts' opinion surveyF Emma, M Cappa, F Antoniazzi, et al.
Physical Review Letters|April 7, 2010
Spectral shape of the two-photon decay of the 2 1S0 state in he-like tinS Trotsenko, A Kumar, A V Volotka, et al.
Ecology and Evolution|April 24, 2025
Mite Domatia and Associated Mite Density in a North American Eastern Deciduous Forest in MichiganCarolyn D K Graham, Lillian R Bailey, Ashley E Cole, et al.
Pageof 138