Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Human genetics

Showing results (621-630 of 11,264) with videos related to

Pageof 1,127
Sort By:
Human Genetics|May 6, 2010
High-density SNP genotyping detects homogeneity of Spanish and French Basques, and confirms their genomic distinctiveness from other European populationsNaiara Rodríguez-Ezpeleta, Jon Alvarez-Busto, Liher Imaz, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Genetics|May 1, 1991
The frequencies of Hbs S and C in Georgia and South CarolinaT H Huisman, H F Harris, A Stewart, et al.
Human Genetics|May 1, 1991
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagenC J Pruchno, D H Cohn, G A Wallis, et al.
Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Human Genetics|May 16, 2009
Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanismsJae Woong Sull, Kung-Yee Liang, Jacqueline B Hetmanski, et al.
Human Genetics|May 4, 2010
The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancerSteven J Hawken, Celia M T Greenwood, Thomas J Hudson, et al.
Human Genetics|May 4, 2010
Copy number variants at Williams-Beuren syndrome 7q11.23 regionGiuseppe Merla, Nicola Brunetti-Pierri, Lucia Micale, et al.
Human Genetics|August 1, 2009
Novel human pathological mutations. Gene symbol: HEXA. Disease: Tay-Sachs diseaseEphrem Chin, L Bean, B Coffee, et al.
Human Genetics|August 5, 2009
The combined impact of metabolic gene polymorphisms on elite endurance athlete status and related phenotypesIldus I Ahmetov, Alun G Williams, Daniil V Popov, et al.
Pageof 1,127

Showing results (621-630 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|May 6, 2010
High-density SNP genotyping detects homogeneity of Spanish and French Basques, and confirms their genomic distinctiveness from other European populationsNaiara Rodríguez-Ezpeleta, Jon Alvarez-Busto, Liher Imaz, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Genetics|May 1, 1991
The frequencies of Hbs S and C in Georgia and South CarolinaT H Huisman, H F Harris, A Stewart, et al.
Human Genetics|May 1, 1991
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagenC J Pruchno, D H Cohn, G A Wallis, et al.
Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Human Genetics|May 16, 2009
Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanismsJae Woong Sull, Kung-Yee Liang, Jacqueline B Hetmanski, et al.
Human Genetics|May 4, 2010
The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancerSteven J Hawken, Celia M T Greenwood, Thomas J Hudson, et al.
Human Genetics|May 4, 2010
Copy number variants at Williams-Beuren syndrome 7q11.23 regionGiuseppe Merla, Nicola Brunetti-Pierri, Lucia Micale, et al.
Human Genetics|August 1, 2009
Novel human pathological mutations. Gene symbol: HEXA. Disease: Tay-Sachs diseaseEphrem Chin, L Bean, B Coffee, et al.
Human Genetics|August 5, 2009
The combined impact of metabolic gene polymorphisms on elite endurance athlete status and related phenotypesIldus I Ahmetov, Alun G Williams, Daniil V Popov, et al.
Pageof 1,127