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Human genetics

Showing results (131-140 of 11,257) with videos related to

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Human Genetics|July 1, 1986
The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphomaA A Kennaugh, S V Butterworth, R Hollis, et al.
Human Genetics|January 20, 2022
Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart diseaseWeicheng Chen, Yuan Zhang, Libing Shen, et al.
Human Genetics|January 20, 2022
Genetic etiology of hearing loss in IranMojgan Babanejad, Maryam Beheshtian, Fereshteh Jamshidi, et al.
Human Genetics|July 1, 1988
Comparison between the allelic frequency distribution of the Ha-ras 1 locus in normal individuals and patients with lymphoma, breast, and ovarian cancerB Corell, B Zoll
Human Genetics|July 1, 1988
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS)C Neidlinger, G Assum, W Krone, et al.
Human Genetics|September 1, 1988
HLA class I and H ferritin gene polymorphisms in normal subjects and patients with haemochromatosisS J Cragg, C Darke, M Worwood
Human Genetics|August 1, 1988
Immunoprecipitation of a male-specific polypeptide after in vitro translation of testicular poly(A)+ RNAU Lattermann, U Müller
Human Genetics|March 21, 2021
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adultsShadi Ahmadmehrabi, Binglan Li, Joseph Park, et al.
Human Genetics|September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystoniaJose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Human Genetics|October 4, 2011
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IIHua Zhang, Hongsheng Chen, Hunjin Luo, et al.
Pageof 1,126

Showing results (131-140 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|July 1, 1986
The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphomaA A Kennaugh, S V Butterworth, R Hollis, et al.
Human Genetics|January 20, 2022
Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart diseaseWeicheng Chen, Yuan Zhang, Libing Shen, et al.
Human Genetics|January 20, 2022
Genetic etiology of hearing loss in IranMojgan Babanejad, Maryam Beheshtian, Fereshteh Jamshidi, et al.
Human Genetics|July 1, 1988
Comparison between the allelic frequency distribution of the Ha-ras 1 locus in normal individuals and patients with lymphoma, breast, and ovarian cancerB Corell, B Zoll
Human Genetics|July 1, 1988
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS)C Neidlinger, G Assum, W Krone, et al.
Human Genetics|September 1, 1988
HLA class I and H ferritin gene polymorphisms in normal subjects and patients with haemochromatosisS J Cragg, C Darke, M Worwood
Human Genetics|August 1, 1988
Immunoprecipitation of a male-specific polypeptide after in vitro translation of testicular poly(A)+ RNAU Lattermann, U Müller
Human Genetics|March 21, 2021
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adultsShadi Ahmadmehrabi, Binglan Li, Joseph Park, et al.
Human Genetics|September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystoniaJose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Human Genetics|October 4, 2011
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IIHua Zhang, Hongsheng Chen, Hunjin Luo, et al.
Pageof 1,126