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Human genetics

Showing results (1211-1220 of 9,569) with videos related to

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Human Genetics|November 4, 2018
Ways of improving precise knock-in by genome-editing technologiesSvetlana A Smirnikhina, Arina A Anuchina, Alexander V Lavrov
Human Genetics|May 1, 1986
Ganglioside GM1 metabolism in living human fibroblasts with beta-galactosidase deficiencyG M Mancini, A T Hoogeveen, H Galjaard, et al.
Human Genetics|December 20, 2021
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variantsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|November 28, 2021
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in EurasiaAisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, et al.
Human Genetics|December 1, 1987
Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridizationJ E Landegent, N Jansen in de Wal, R W Dirks, et al.
Human Genetics|November 10, 2021
Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variantSateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics|July 21, 2019
DNA damage in aging, the stem cell perspectiveTaylor McNeely, Michael Leone, Hagai Yanai, et al.
Human Genetics|July 31, 2019
Correction to: Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic historiesFrancisco C Ceballos, Scott Hazelhurst, Michèle Ramsay
Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB Nedelec, J-M Rozet, L Fares Taie
Human Genetics|July 1, 1988
Regional chromosomal localisation of APOA2 to 1q21-1q23H R Middleton-Price, J A van den Berghe, J Scott, et al.
Pageof 957

Showing results (1211-1220 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|November 4, 2018
Ways of improving precise knock-in by genome-editing technologiesSvetlana A Smirnikhina, Arina A Anuchina, Alexander V Lavrov
Human Genetics|May 1, 1986
Ganglioside GM1 metabolism in living human fibroblasts with beta-galactosidase deficiencyG M Mancini, A T Hoogeveen, H Galjaard, et al.
Human Genetics|December 20, 2021
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variantsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|November 28, 2021
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in EurasiaAisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, et al.
Human Genetics|December 1, 1987
Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridizationJ E Landegent, N Jansen in de Wal, R W Dirks, et al.
Human Genetics|November 10, 2021
Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variantSateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics|July 21, 2019
DNA damage in aging, the stem cell perspectiveTaylor McNeely, Michael Leone, Hagai Yanai, et al.
Human Genetics|July 31, 2019
Correction to: Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic historiesFrancisco C Ceballos, Scott Hazelhurst, Michèle Ramsay
Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB Nedelec, J-M Rozet, L Fares Taie
Human Genetics|July 1, 1988
Regional chromosomal localisation of APOA2 to 1q21-1q23H R Middleton-Price, J A van den Berghe, J Scott, et al.
Pageof 957