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Matthew B Dobbs

Showing results (141-150 of 165) with videos related to

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Human Molecular Genetics|July 22, 2011
Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in miceDavid M Alvarado, Kevin McCall, Hyuliya Aferol, et al.
Journal of Neurosurgery. Pediatrics|April 11, 2020
Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformationGabe Haller, Brooke Sadler, Timothy Kuensting, et al.
Journal of Pediatric Orthopedics. Part B|September 16, 2016
Design and descriptive data of the randomized Clubfoot Foot Abduction Brace Length of Treatment Study (FAB24)Matthew B Dobbs, Steven L Frick, Vincent S Mosca, et al.
Journal of Pediatric Orthopedics|April 18, 2018
What Factors Influence Union and Refracture of Congenital Pseudarthrosis of the Tibia? A Multicenter Long-term StudyHitesh Shah, Benjamin Joseph, Binu V S Nair, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 2, 2006
HOXD10 M319K mutation in a family with isolated congenital vertical talusMatthew B Dobbs, Christina A Gurnett, Brandon Pierce, et al.
Journal of Medical Genetics|March 27, 2014
Genome-wide association study identifies new disease loci for isolated clubfootTian-Xiao Zhang, Gabe Haller, Peng Lin, et al.
The Journal of Bone and Joint Surgery. American Volume|September 4, 2015
Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic ScoliosisGabe Haller, David M Alvarado, Marcia C Willing, et al.
Clinical Orthopaedics and Related Research|March 14, 2018
Editorial: The Complexity of Reporting Race and Ethnicity in Orthopaedic ResearchSeth S Leopold, Lee Beadling, Anthony M Calabro, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Variants in genes that encode muscle contractile proteins influence risk for isolated clubfootKatelyn S Weymouth, Susan H Blanton, Michael J Bamshad, et al.
Human Molecular Genetics|November 15, 2015
A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosisGabe Haller, David Alvarado, Kevin Mccall, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|July 22, 2011
Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in miceDavid M Alvarado, Kevin McCall, Hyuliya Aferol, et al.
Journal of Neurosurgery. Pediatrics|April 11, 2020
Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformationGabe Haller, Brooke Sadler, Timothy Kuensting, et al.
Journal of Pediatric Orthopedics. Part B|September 16, 2016
Design and descriptive data of the randomized Clubfoot Foot Abduction Brace Length of Treatment Study (FAB24)Matthew B Dobbs, Steven L Frick, Vincent S Mosca, et al.
Journal of Pediatric Orthopedics|April 18, 2018
What Factors Influence Union and Refracture of Congenital Pseudarthrosis of the Tibia? A Multicenter Long-term StudyHitesh Shah, Benjamin Joseph, Binu V S Nair, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 2, 2006
HOXD10 M319K mutation in a family with isolated congenital vertical talusMatthew B Dobbs, Christina A Gurnett, Brandon Pierce, et al.
Journal of Medical Genetics|March 27, 2014
Genome-wide association study identifies new disease loci for isolated clubfootTian-Xiao Zhang, Gabe Haller, Peng Lin, et al.
The Journal of Bone and Joint Surgery. American Volume|September 4, 2015
Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic ScoliosisGabe Haller, David M Alvarado, Marcia C Willing, et al.
Clinical Orthopaedics and Related Research|March 14, 2018
Editorial: The Complexity of Reporting Race and Ethnicity in Orthopaedic ResearchSeth S Leopold, Lee Beadling, Anthony M Calabro, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Variants in genes that encode muscle contractile proteins influence risk for isolated clubfootKatelyn S Weymouth, Susan H Blanton, Michael J Bamshad, et al.
Human Molecular Genetics|November 15, 2015
A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosisGabe Haller, David Alvarado, Kevin Mccall, et al.
Pageof 17