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Human genetics

Showing results (151-160 of 11,257) with videos related to

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Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutanea tardaValentina Brancaleoni, Elena Di Pierro, Valeria Moriondo, et al.
Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: PPT1. Disease: neuronal ceroid lipofuscinosis, juvenileO Thomas Mueller, A Coovadia
Human Genetics|July 16, 2011
Meta-analysis of new genome-wide association studies of colorectal cancer riskUlrike Peters, Carolyn M Hutter, Li Hsu, et al.
Human Genetics|December 1, 1990
The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndromeM Gessler, H Hameister, I Henry, et al.
Human Genetics|July 26, 2011
From single biobanks to international networks: developing e-governanceJane Kaye
Human Genetics|December 18, 1978
Appearance of hCG-receptor after conversion of newborn ovarian cells into testicular structures by H-Y antigen in vitroU Müller, M T Zenzes, T Bauknecht, et al.
Human Genetics|August 23, 2011
Sex differences in disease risk from reported genome-wide association study findingsLinda Y Liu, Marc A Schaub, Marina Sirota, et al.
Human Genetics|August 31, 2011
Novel Alu retrotransposon insertion leading to Alström syndromeMustafa Taşkesen, Gayle B Collin, Alexei V Evsikov, et al.
Human Genetics|July 8, 2011
Artifact due to differential error when cases and controls are imputed from different platformsJennifer A Sinnott, Peter Kraft
Human Genetics|July 8, 2011
Common variants for atrial fibrillation: results from genome-wide association studiesXinyuan Liu, Fei Wang, Ashley C Knight, et al.
Pageof 1,126

Showing results (151-160 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutanea tardaValentina Brancaleoni, Elena Di Pierro, Valeria Moriondo, et al.
Human Genetics|April 15, 2011
Novel human pathological mutations. Gene symbol: PPT1. Disease: neuronal ceroid lipofuscinosis, juvenileO Thomas Mueller, A Coovadia
Human Genetics|July 16, 2011
Meta-analysis of new genome-wide association studies of colorectal cancer riskUlrike Peters, Carolyn M Hutter, Li Hsu, et al.
Human Genetics|December 1, 1990
The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndromeM Gessler, H Hameister, I Henry, et al.
Human Genetics|July 26, 2011
From single biobanks to international networks: developing e-governanceJane Kaye
Human Genetics|December 18, 1978
Appearance of hCG-receptor after conversion of newborn ovarian cells into testicular structures by H-Y antigen in vitroU Müller, M T Zenzes, T Bauknecht, et al.
Human Genetics|August 23, 2011
Sex differences in disease risk from reported genome-wide association study findingsLinda Y Liu, Marc A Schaub, Marina Sirota, et al.
Human Genetics|August 31, 2011
Novel Alu retrotransposon insertion leading to Alström syndromeMustafa Taşkesen, Gayle B Collin, Alexei V Evsikov, et al.
Human Genetics|July 8, 2011
Artifact due to differential error when cases and controls are imputed from different platformsJennifer A Sinnott, Peter Kraft
Human Genetics|July 8, 2011
Common variants for atrial fibrillation: results from genome-wide association studiesXinyuan Liu, Fei Wang, Ashley C Knight, et al.
Pageof 1,126