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Showing results (141-150 of 223) with videos related to

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Neurobiology of Aging|February 4, 2018
An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease riskShuquan Rao, Mahdi Ghani, Zhiyun Guo, et al.
Biotechniques|February 3, 2007
SNP-based chromosomal copy number ascertainment following multiple displacement whole-genome amplificationJason J Corneveaux, Michael C Kruer, Diane Hu-Lince, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Molecular Psychiatry|May 3, 2002
No missense mutation of WKL1 in a subgroup of probands with schizophreniaJ M Devaney, E A Donarum, K M Brown, et al.
Bioinformatics (Oxford, England)|October 26, 2006
SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arraysJianping Hua, David W Craig, Marcel Brun, et al.
Epilepsy Research|May 22, 2007
Chromosomal abnormality at 6p25.1-25.3 identifies a susceptibility locus for hypothalamic hamartoma associated with epilepsyJohn F Kerrigan, Michael C Kruer, Jason Corneveaux, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences|October 2, 1998
Group report: emergent properties of natural and artificial systemsS Reimann, J M Fuster, A Gierer, et al.
American Journal of Human Genetics|February 7, 2008
Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locusDavid W Craig, Abraham Itty, Corrie Panganiban, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite populationKevin A Strauss, Erik G Puffenberger, David W Craig, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Pageof 23

Showing results (141-150 of 223) with videos related to

Sort By:
Pageof 23
Neurobiology of Aging|February 4, 2018
An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease riskShuquan Rao, Mahdi Ghani, Zhiyun Guo, et al.
Biotechniques|February 3, 2007
SNP-based chromosomal copy number ascertainment following multiple displacement whole-genome amplificationJason J Corneveaux, Michael C Kruer, Diane Hu-Lince, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Molecular Psychiatry|May 3, 2002
No missense mutation of WKL1 in a subgroup of probands with schizophreniaJ M Devaney, E A Donarum, K M Brown, et al.
Bioinformatics (Oxford, England)|October 26, 2006
SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arraysJianping Hua, David W Craig, Marcel Brun, et al.
Epilepsy Research|May 22, 2007
Chromosomal abnormality at 6p25.1-25.3 identifies a susceptibility locus for hypothalamic hamartoma associated with epilepsyJohn F Kerrigan, Michael C Kruer, Jason Corneveaux, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences|October 2, 1998
Group report: emergent properties of natural and artificial systemsS Reimann, J M Fuster, A Gierer, et al.
American Journal of Human Genetics|February 7, 2008
Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locusDavid W Craig, Abraham Itty, Corrie Panganiban, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite populationKevin A Strauss, Erik G Puffenberger, David W Craig, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Pageof 23