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David Gurwitz

Showing results (91-100 of 98) with videos related to

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American Journal of Human Genetics|January 13, 2006
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder eventDoron M Behar, Ene Metspalu, Toomas Kivisild, et al.
Annals of Human Genetics|May 22, 2009
Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variantHui Li, Svetlana Borinskaya, Kimio Yoshimura, et al.
Human Genetics|November 9, 2011
A global view of the OCA2-HERC2 region and pigmentationMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
Nature|June 10, 2010
The genome-wide structure of the Jewish peopleDoron M Behar, Bayazit Yunusbayev, Mait Metspalu, et al.
Pharmacogenomics|June 29, 2019
Pharmacogenomics education in medical and pharmacy schools: conclusions of a global surveyNataša Karas Kuželički, Irena Prodan Žitnik, David Gurwitz, et al.
American Journal of Human Genetics|February 2, 2010
The distribution and most recent common ancestor of the 17q21 inversion in humansMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
European Journal of Human Genetics : EJHG|December 25, 2014
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseasesMarina Mora, Corrado Angelini, Fabrizia Bignami, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
American Journal of Human Genetics|January 13, 2006
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder eventDoron M Behar, Ene Metspalu, Toomas Kivisild, et al.
Annals of Human Genetics|May 22, 2009
Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variantHui Li, Svetlana Borinskaya, Kimio Yoshimura, et al.
Human Genetics|November 9, 2011
A global view of the OCA2-HERC2 region and pigmentationMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
Nature|June 10, 2010
The genome-wide structure of the Jewish peopleDoron M Behar, Bayazit Yunusbayev, Mait Metspalu, et al.
Pharmacogenomics|June 29, 2019
Pharmacogenomics education in medical and pharmacy schools: conclusions of a global surveyNataša Karas Kuželički, Irena Prodan Žitnik, David Gurwitz, et al.
American Journal of Human Genetics|February 2, 2010
The distribution and most recent common ancestor of the 17q21 inversion in humansMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
European Journal of Human Genetics : EJHG|December 25, 2014
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseasesMarina Mora, Corrado Angelini, Fabrizia Bignami, et al.
Pageof 10