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Human genetics

Showing results (251-260 of 11,262) with videos related to

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Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)Susana Ferreira, Rosa S Silva, João Paulo Oliveira
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathyVéronique Vieira, Guillaume de la Houssaye, Anouk Dansault, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: EPM2A. Disease: Lafora progressive myoclonus epilepsyM J Trujillo-Tiebas, M Fenollar-Cortés, P Gómez-Garré, et al.
Human Genetics|April 1, 1986
Ethnic variation in vitamin D-binding protein (GC): a review of isoelectric focusing studies in human populationsM I Kamboh, R E Ferrell
Human Genetics|April 1, 1986
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcomaS Scappaticci, D Cerimele, F Cottoni, et al.
Human Genetics|July 1, 1986
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1A Dubart, M G Mattei, N Raich, et al.
Human Genetics|February 5, 2022
Evolutionary history of type II transmembrane serine proteases involved in viral primingDiego Forni, Manuela Sironi, Rachele Cagliani
Human Genetics|February 1, 1987
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qterS R Dlouhy, J C Christian, J L Haines, et al.
Pageof 1,127

Showing results (251-260 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)Susana Ferreira, Rosa S Silva, João Paulo Oliveira
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathyVéronique Vieira, Guillaume de la Houssaye, Anouk Dansault, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: EPM2A. Disease: Lafora progressive myoclonus epilepsyM J Trujillo-Tiebas, M Fenollar-Cortés, P Gómez-Garré, et al.
Human Genetics|April 1, 1986
Ethnic variation in vitamin D-binding protein (GC): a review of isoelectric focusing studies in human populationsM I Kamboh, R E Ferrell
Human Genetics|April 1, 1986
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcomaS Scappaticci, D Cerimele, F Cottoni, et al.
Human Genetics|July 1, 1986
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1A Dubart, M G Mattei, N Raich, et al.
Human Genetics|February 5, 2022
Evolutionary history of type II transmembrane serine proteases involved in viral primingDiego Forni, Manuela Sironi, Rachele Cagliani
Human Genetics|February 1, 1987
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qterS R Dlouhy, J C Christian, J L Haines, et al.
Pageof 1,127