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L Haines

Showing results (421-430 of 994) with videos related to

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American Journal of Medical Genetics|July 13, 2001
Evidence supporting WNT2 as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
Cell|March 2, 1992
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaA I McClatchey, P Van den Bergh, M A Pericak-Vance, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2010
Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical recordsLogan Dumitrescu, Marylyn D Ritchie, Kristin Brown-Gentry, et al.
Genomics|July 15, 1994
Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic associationH M Mitchison, P E Taschner, A M O'Rawe, et al.
Human Molecular Genetics|December 18, 2007
Deletion of CFHR3 and CFHR1 genes in age-related macular degenerationKylee L Spencer, Michael A Hauser, Lana M Olson, et al.
BMC Medical Genetics|March 7, 2006
Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the AmishJacob L McCauley, Daniel W Hahs, Lan Jiang, et al.
Clinical Genetics|April 30, 2013
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucomaJ L Wiggs, G R Howell, K Linkroum, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Human Molecular Genetics|June 20, 2007
Protective effect of complement factor B and complement component 2 variants in age-related macular degenerationKylee L Spencer, Michael A Hauser, Lana M Olson, et al.
Annals of Human Genetics|August 30, 2007
No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasetsXueying Liang, Nathalie Schnetz-Boutaud, Jackie Bartlett, et al.
Pageof 100

Showing results (421-430 of 994) with videos related to

Sort By:
Pageof 100
American Journal of Medical Genetics|July 13, 2001
Evidence supporting WNT2 as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
Cell|March 2, 1992
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaA I McClatchey, P Van den Bergh, M A Pericak-Vance, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2010
Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical recordsLogan Dumitrescu, Marylyn D Ritchie, Kristin Brown-Gentry, et al.
Genomics|July 15, 1994
Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic associationH M Mitchison, P E Taschner, A M O'Rawe, et al.
Human Molecular Genetics|December 18, 2007
Deletion of CFHR3 and CFHR1 genes in age-related macular degenerationKylee L Spencer, Michael A Hauser, Lana M Olson, et al.
BMC Medical Genetics|March 7, 2006
Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the AmishJacob L McCauley, Daniel W Hahs, Lan Jiang, et al.
Clinical Genetics|April 30, 2013
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucomaJ L Wiggs, G R Howell, K Linkroum, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Human Molecular Genetics|June 20, 2007
Protective effect of complement factor B and complement component 2 variants in age-related macular degenerationKylee L Spencer, Michael A Hauser, Lana M Olson, et al.
Annals of Human Genetics|August 30, 2007
No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasetsXueying Liang, Nathalie Schnetz-Boutaud, Jackie Bartlett, et al.
Pageof 100