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Human genetics

Showing results (951-960 of 9,569) with videos related to

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Human Genetics|November 24, 2016
Regional selection of the brain size regulating gene CASC5 provides new insight into human brain evolutionLei Shi, Enzhi Hu, Zhenbo Wang, et al.
Human Genetics|November 16, 2016
Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disordersR Holt, S A Ugur Iseri, A W Wyatt, et al.
Human Genetics|November 17, 2016
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autismNuria C Bramswig, H-J Lüdecke, M Pettersson, et al.
Human Genetics|December 2, 2016
Mutations in SLC5A6 associated with brain, immune, bone, and intestinal dysfunction in a young childVeedamali S Subramanian, Alexandru R Constantinescu, Paul J Benke, et al.
Human Genetics|October 1, 1989
Population bottlenecks in Polynesia revealed by minisatellitesJ Flint, A J Boyce, J J Martinson, et al.
Human Genetics|October 1, 1989
Chromosome abnormalities in early pregnancy analyzed by direct chromosome preparation of chorionic villiX T Zhou, H S Tong, S G Wong, et al.
Human Genetics|October 1, 1989
Trisomy 18 in monozygotic twinsA F Mulder, J van Eyck, F Groenendaal, et al.
Human Genetics|October 1, 1989
Deletion 3q27----3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miliaria rubra-like lesionsI Jokiaho, A Salo, K M Niemi, et al.
Human Genetics|March 25, 2017
Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosisAnthony L Traboulsee, A Dessa Sadovnick, Mary Encarnacion, et al.
Human Genetics|March 29, 2017
Detecting past male-mediated expansions using the Y chromosomeChiara Batini, Mark A Jobling
Pageof 957

Showing results (951-960 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|November 24, 2016
Regional selection of the brain size regulating gene CASC5 provides new insight into human brain evolutionLei Shi, Enzhi Hu, Zhenbo Wang, et al.
Human Genetics|November 16, 2016
Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disordersR Holt, S A Ugur Iseri, A W Wyatt, et al.
Human Genetics|November 17, 2016
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autismNuria C Bramswig, H-J Lüdecke, M Pettersson, et al.
Human Genetics|December 2, 2016
Mutations in SLC5A6 associated with brain, immune, bone, and intestinal dysfunction in a young childVeedamali S Subramanian, Alexandru R Constantinescu, Paul J Benke, et al.
Human Genetics|October 1, 1989
Population bottlenecks in Polynesia revealed by minisatellitesJ Flint, A J Boyce, J J Martinson, et al.
Human Genetics|October 1, 1989
Chromosome abnormalities in early pregnancy analyzed by direct chromosome preparation of chorionic villiX T Zhou, H S Tong, S G Wong, et al.
Human Genetics|October 1, 1989
Trisomy 18 in monozygotic twinsA F Mulder, J van Eyck, F Groenendaal, et al.
Human Genetics|October 1, 1989
Deletion 3q27----3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miliaria rubra-like lesionsI Jokiaho, A Salo, K M Niemi, et al.
Human Genetics|March 25, 2017
Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosisAnthony L Traboulsee, A Dessa Sadovnick, Mary Encarnacion, et al.
Human Genetics|March 29, 2017
Detecting past male-mediated expansions using the Y chromosomeChiara Batini, Mark A Jobling
Pageof 957