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T Gordon

Showing results (651-660 of 700) with videos related to

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American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
The Journal of the American Academy of Orthopaedic Surgeons|August 7, 2012
Reprioritization of research for combat casualty careJames R Ficke, William T Obremskey, Robert J Gaines, et al.
Science (New York, N.Y.)|August 25, 2004
Regions of strong coupling between soil moisture and precipitationRandal D Koster, Paul A Dirmeyer, Zhichang Guo, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndromeVanessa L Romanelli Tavares, Roseli M Zechi-Ceide, Debora R Bertola, et al.
European Journal of Human Genetics : EJHG|July 17, 2014
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effectVanessa L Romanelli Tavares, Christopher T Gordon, Roseli M Zechi-Ceide, et al.
Plos Biology|December 31, 2014
Structured inquiry-based learning: Drosophila GAL4 enhancer trap characterization in an undergraduate laboratory courseChristopher R Dunne, Anthony R Cillo, Danielle R Glick, et al.
Nature Communications|February 6, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidineVíctor Faundes, Martin D Jennings, Siobhan Crilly, et al.
Nature Communications|August 8, 2018
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defectsJohanne Dubail, Céline Huber, Sandrine Chantepie, et al.
European Journal of Human Genetics : EJHG|January 14, 2018
Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndromeJean-Luc Alessandri, Christopher T Gordon, Marie-Line Jacquemont, et al.
American Journal of Human Genetics|August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in InfancyAnne Guimier, Christopher T Gordon, François Godard, et al.
Pageof 70

Showing results (651-660 of 700) with videos related to

Sort By:
Pageof 70
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
The Journal of the American Academy of Orthopaedic Surgeons|August 7, 2012
Reprioritization of research for combat casualty careJames R Ficke, William T Obremskey, Robert J Gaines, et al.
Science (New York, N.Y.)|August 25, 2004
Regions of strong coupling between soil moisture and precipitationRandal D Koster, Paul A Dirmeyer, Zhichang Guo, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndromeVanessa L Romanelli Tavares, Roseli M Zechi-Ceide, Debora R Bertola, et al.
European Journal of Human Genetics : EJHG|July 17, 2014
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effectVanessa L Romanelli Tavares, Christopher T Gordon, Roseli M Zechi-Ceide, et al.
Plos Biology|December 31, 2014
Structured inquiry-based learning: Drosophila GAL4 enhancer trap characterization in an undergraduate laboratory courseChristopher R Dunne, Anthony R Cillo, Danielle R Glick, et al.
Nature Communications|February 6, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidineVíctor Faundes, Martin D Jennings, Siobhan Crilly, et al.
Nature Communications|August 8, 2018
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defectsJohanne Dubail, Céline Huber, Sandrine Chantepie, et al.
European Journal of Human Genetics : EJHG|January 14, 2018
Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndromeJean-Luc Alessandri, Christopher T Gordon, Marie-Line Jacquemont, et al.
American Journal of Human Genetics|August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in InfancyAnne Guimier, Christopher T Gordon, François Godard, et al.
Pageof 70