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L Haines

Showing results (381-390 of 994) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993D J Kwiatkowski, J Armour, A E Bale, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23L A Janssen, S Povey, J Attwood, et al.
Annals of Neurology|June 1, 1996
Alzheimer's disease and apolipoprotein E-4 allele in an Amish populationM A Pericak-Vance, C C Johnson, J B Rimmler, et al.
Neuron|August 1, 1989
Recombination events suggest potential sites for the Huntington's disease geneM E MacDonald, J L Haines, M Zimmer, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisRazaq O Durodoye, Timothy H Ciesielski, Penelope Benchek, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Human Molecular Genetics|November 1, 1992
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)D H Donaldson, D R Rosen, J O'Regan, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative DiseaseMichelle Grunin, Ellen Palmer, Sarah de Jong, et al.
Investigative Ophthalmology & Visual Science|August 17, 2017
Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1Patrice J Persad, Iris M Heid, Daniel E Weeks, et al.
Pageof 100

Showing results (381-390 of 994) with videos related to

Sort By:
Pageof 100
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993D J Kwiatkowski, J Armour, A E Bale, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23L A Janssen, S Povey, J Attwood, et al.
Annals of Neurology|June 1, 1996
Alzheimer's disease and apolipoprotein E-4 allele in an Amish populationM A Pericak-Vance, C C Johnson, J B Rimmler, et al.
Neuron|August 1, 1989
Recombination events suggest potential sites for the Huntington's disease geneM E MacDonald, J L Haines, M Zimmer, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisRazaq O Durodoye, Timothy H Ciesielski, Penelope Benchek, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Human Molecular Genetics|November 1, 1992
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)D H Donaldson, D R Rosen, J O'Regan, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative DiseaseMichelle Grunin, Ellen Palmer, Sarah de Jong, et al.
Investigative Ophthalmology & Visual Science|August 17, 2017
Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1Patrice J Persad, Iris M Heid, Daniel E Weeks, et al.
Pageof 100