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L Mandel

Showing results (291-300 of 451) with videos related to

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Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
Ophthalmic Genetics|October 19, 2011
Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencingK Aliferis, S Hellé, G Gyapay, et al.
Annals of Emergency Medicine|February 1, 1993
Education in adult basic life support training programsL S Flint, J E Billi, K Kelly, et al.
American Journal of Human Genetics|June 1, 1996
Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophyV Feigenbaum, G Lombard-Platet, S Guidoux, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Genetic mapping of the human X chromosome by using restriction fragment length polymorphismsD Drayna, K Davies, D Hartley, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.
American Journal of Human Genetics|February 1, 1988
Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesB Arveiler, I Oberlé, A Vincent, et al.
The EMBO Journal|July 1, 1985
Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.
Innovations (Philadelphia, Pa.)|March 23, 2022
Use of Percutaneous Cannulation in Robotic Mitral Valve SurgeryJake L Rosen, Kyle W Prochno, Colin C Yost, et al.
Pageof 46

Showing results (291-300 of 451) with videos related to

Sort By:
Pageof 46
Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
Ophthalmic Genetics|October 19, 2011
Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencingK Aliferis, S Hellé, G Gyapay, et al.
Annals of Emergency Medicine|February 1, 1993
Education in adult basic life support training programsL S Flint, J E Billi, K Kelly, et al.
American Journal of Human Genetics|June 1, 1996
Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophyV Feigenbaum, G Lombard-Platet, S Guidoux, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Genetic mapping of the human X chromosome by using restriction fragment length polymorphismsD Drayna, K Davies, D Hartley, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.
American Journal of Human Genetics|February 1, 1988
Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesB Arveiler, I Oberlé, A Vincent, et al.
The EMBO Journal|July 1, 1985
Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.
Innovations (Philadelphia, Pa.)|March 23, 2022
Use of Percutaneous Cannulation in Robotic Mitral Valve SurgeryJake L Rosen, Kyle W Prochno, Colin C Yost, et al.
Pageof 46