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James L Weber

Showing results (1-10 of 28) with videos related to

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Nature Genetics|June 8, 2002
The Iceland mapJames L Weber
Biology Direct|June 8, 2006
Clinical applications of Genome Polymorphism ScansJames L Weber
American Journal of Human Genetics|April 22, 2008
Linkage disequilibrium between STRPs and SNPs across the human genomeBret A Payseur, Michael Place, James L Weber
Molecular Vision|April 8, 2024
Clinical sequencing of the retinitis pigmentosa gene <i>RPGR</i> in over 1,000 cases of vision lossMadhulatha Pantrangi, Julie Rath, Nicole Kaetterhenry, et al.
BMC Genomics|February 26, 2003
STRP screening sets for the human genome at 5 cM densityNader Ghebranious, David Vaske, Adong Yu, et al.
American Journal of Human Genetics|September 3, 2002
Human diallelic insertion/deletion polymorphismsJames L Weber, Donna David, Jeremy Heil, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2011
A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformationsCarol J Gallione, Ann Solatycki, Issam A Awad, et al.
Molecular Biotechnology|January 26, 2008
Channel glass-based detection of human short insertion/deletion polymorphisms by tandem hybridizationGabriel Betanzos-Cabrera, Brent W Harker, Mitchel J Doktycz, et al.
Molecular Biotechnology|December 21, 2007
A comparison of hybridization efficiency between flat glass and channel glass solid supportsGabriel Betanzos-Cabrera, Brent W Harker, Mitchel J Doktycz, et al.
Human Mutation|January 24, 2006
Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disordersPeng Xiao, Pengyuan Liu, James L Weber, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Nature Genetics|June 8, 2002
The Iceland mapJames L Weber
Biology Direct|June 8, 2006
Clinical applications of Genome Polymorphism ScansJames L Weber
American Journal of Human Genetics|April 22, 2008
Linkage disequilibrium between STRPs and SNPs across the human genomeBret A Payseur, Michael Place, James L Weber
Molecular Vision|April 8, 2024
Clinical sequencing of the retinitis pigmentosa gene <i>RPGR</i> in over 1,000 cases of vision lossMadhulatha Pantrangi, Julie Rath, Nicole Kaetterhenry, et al.
BMC Genomics|February 26, 2003
STRP screening sets for the human genome at 5 cM densityNader Ghebranious, David Vaske, Adong Yu, et al.
American Journal of Human Genetics|September 3, 2002
Human diallelic insertion/deletion polymorphismsJames L Weber, Donna David, Jeremy Heil, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2011
A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformationsCarol J Gallione, Ann Solatycki, Issam A Awad, et al.
Molecular Biotechnology|January 26, 2008
Channel glass-based detection of human short insertion/deletion polymorphisms by tandem hybridizationGabriel Betanzos-Cabrera, Brent W Harker, Mitchel J Doktycz, et al.
Molecular Biotechnology|December 21, 2007
A comparison of hybridization efficiency between flat glass and channel glass solid supportsGabriel Betanzos-Cabrera, Brent W Harker, Mitchel J Doktycz, et al.
Human Mutation|January 24, 2006
Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disordersPeng Xiao, Pengyuan Liu, James L Weber, et al.
Pageof 3