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Showing results (381-390 of 431) with videos related to

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European Journal of Human Genetics : EJHG|June 30, 2011
Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasiaVerónica Barca-Tierno, Miriam Aza-Carmona, Eva Barroso, et al.
Human Genetics|October 1, 2011
Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human heightJae-Jung Kim, Young-Mi Park, Kyu-Heum Baik, et al.
American Journal of Medical Genetics. Part A|February 26, 2015
Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterizationFe Amalia García-Santiago, Víctor Martínez-Glez, Fernando Santos, et al.
The New England Journal of Medicine|December 9, 2015
A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive EventsMatthew M Heeney, Carolyn C Hoppe, Miguel R Abboud, et al.
Human Molecular Genetics|April 25, 2015
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the ciliumJosé A Caparrós-Martín, Alessandro De Luca, François Cartault, et al.
Community Science|March 12, 2026
What Does Equitable Co-Production Entail? Three PerspectivesK L Akerlof, K M F Timm, A Chase, et al.
Blood|December 4, 2015
Rapid expansion of preexisting nonleukemic hematopoietic clones frequently follows induction therapy for de novo AMLTerrence N Wong, Christopher A Miller, Jeffery M Klco, et al.
JCI Insight|March 9, 2018
Subclones dominate at MDS progression following allogeneic hematopoietic cell transplantMeagan A Jacoby, Eric J Duncavage, Gue Su Chang, et al.
Talanta|July 1, 2008
First interlaboratory exercise on non-steroidal anti-inflammatory drugs analysis in environmental samplesM Farré, M Petrovic, M Gros, et al.
Blood|December 28, 2007
Identification of somatic JAK1 mutations in patients with acute myeloid leukemiaZhifu Xiang, Yu Zhao, Vesselin Mitaksov, et al.
Pageof 44

Showing results (381-390 of 431) with videos related to

Sort By:
Pageof 44
European Journal of Human Genetics : EJHG|June 30, 2011
Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasiaVerónica Barca-Tierno, Miriam Aza-Carmona, Eva Barroso, et al.
Human Genetics|October 1, 2011
Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human heightJae-Jung Kim, Young-Mi Park, Kyu-Heum Baik, et al.
American Journal of Medical Genetics. Part A|February 26, 2015
Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterizationFe Amalia García-Santiago, Víctor Martínez-Glez, Fernando Santos, et al.
The New England Journal of Medicine|December 9, 2015
A Multinational Trial of Prasugrel for Sickle Cell Vaso-Occlusive EventsMatthew M Heeney, Carolyn C Hoppe, Miguel R Abboud, et al.
Human Molecular Genetics|April 25, 2015
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the ciliumJosé A Caparrós-Martín, Alessandro De Luca, François Cartault, et al.
Community Science|March 12, 2026
What Does Equitable Co-Production Entail? Three PerspectivesK L Akerlof, K M F Timm, A Chase, et al.
Blood|December 4, 2015
Rapid expansion of preexisting nonleukemic hematopoietic clones frequently follows induction therapy for de novo AMLTerrence N Wong, Christopher A Miller, Jeffery M Klco, et al.
JCI Insight|March 9, 2018
Subclones dominate at MDS progression following allogeneic hematopoietic cell transplantMeagan A Jacoby, Eric J Duncavage, Gue Su Chang, et al.
Talanta|July 1, 2008
First interlaboratory exercise on non-steroidal anti-inflammatory drugs analysis in environmental samplesM Farré, M Petrovic, M Gros, et al.
Blood|December 28, 2007
Identification of somatic JAK1 mutations in patients with acute myeloid leukemiaZhifu Xiang, Yu Zhao, Vesselin Mitaksov, et al.
Pageof 44