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Damian Labuda

Showing results (71-80 of 83) with videos related to

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Journal of Medical Genetics|September 27, 2012
Mutations in TMEM231 cause Joubert syndrome in French CanadiansMyriam Srour, Fadi F Hamdan, Jeremy A Schwartzentruber, et al.
Molecular Biology and Evolution|January 27, 2011
An X-linked haplotype of Neandertal origin is present among all non-African populationsVania Yotova, Jean-Francois Lefebvre, Claudia Moreau, et al.
American Journal of Human Genetics|March 20, 2012
Mutations in C5ORF42 cause Joubert syndrome in the French Canadian populationMyriam Srour, Jeremy Schwartzentruber, Fadi F Hamdan, et al.
American Journal of Human Genetics|August 6, 2003
Y-chromosome evidence for differing ancient demographic histories in the AmericasMaria-Catira Bortolini, Francisco M Salzano, Mark G Thomas, et al.
American Journal of Human Genetics|September 7, 2010
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implicationsKaye N Ballantyne, Miriam Goedbloed, Rixun Fang, et al.
Plos Genetics|November 28, 2007
Genetic variation and population structure in native AmericansSijia Wang, Cecil M Lewis, Mattias Jakobsson, et al.
Annals of Human Genetics|October 5, 2010
Contrasting patterns of nuclear and mtDNA diversity in Native American populationsNing Ning Yang, Stephane Mazières, Claudio Bravi, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
American Journal of Human Genetics|October 20, 2015
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104Myriam Srour, Fadi F Hamdan, Dianalee McKnight, et al.
Science (New York, N.Y.)|August 8, 2015
Global diversity, population stratification, and selection of human copy-number variationPeter H Sudmant, Swapan Mallick, Bradley J Nelson, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|September 27, 2012
Mutations in TMEM231 cause Joubert syndrome in French CanadiansMyriam Srour, Fadi F Hamdan, Jeremy A Schwartzentruber, et al.
Molecular Biology and Evolution|January 27, 2011
An X-linked haplotype of Neandertal origin is present among all non-African populationsVania Yotova, Jean-Francois Lefebvre, Claudia Moreau, et al.
American Journal of Human Genetics|March 20, 2012
Mutations in C5ORF42 cause Joubert syndrome in the French Canadian populationMyriam Srour, Jeremy Schwartzentruber, Fadi F Hamdan, et al.
American Journal of Human Genetics|August 6, 2003
Y-chromosome evidence for differing ancient demographic histories in the AmericasMaria-Catira Bortolini, Francisco M Salzano, Mark G Thomas, et al.
American Journal of Human Genetics|September 7, 2010
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implicationsKaye N Ballantyne, Miriam Goedbloed, Rixun Fang, et al.
Plos Genetics|November 28, 2007
Genetic variation and population structure in native AmericansSijia Wang, Cecil M Lewis, Mattias Jakobsson, et al.
Annals of Human Genetics|October 5, 2010
Contrasting patterns of nuclear and mtDNA diversity in Native American populationsNing Ning Yang, Stephane Mazières, Claudio Bravi, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
American Journal of Human Genetics|October 20, 2015
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104Myriam Srour, Fadi F Hamdan, Dianalee McKnight, et al.
Science (New York, N.Y.)|August 8, 2015
Global diversity, population stratification, and selection of human copy-number variationPeter H Sudmant, Swapan Mallick, Bradley J Nelson, et al.
Pageof 9