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Showing results (201-210 of 218) with videos related to

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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.
Human Molecular Genetics|January 5, 2010
Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1Christina A Gurnett, David M Desruisseau, Kevin McCall, et al.
Biology of Reproduction|July 16, 2016
Identification of Beef Heifers with Superior Uterine Capacity for PregnancyThomas W Geary, Gregory W Burns, Joao G N Moraes, et al.
Nature Reviews. Disease Primers|May 19, 2016
Adolescent idiopathic scoliosisJack C Cheng, René M Castelein, Winnie C Chu, et al.
G3 (Bethesda, Md.)|December 16, 2014
Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosisErin E Baschal, Cambria I Wethey, Kandice Swindle, et al.
Spine Deformity|November 17, 2019
Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST): Development and Validation of a Prognostic Model in Untreated Adolescent Idiopathic Scoliosis Using the Simplified Skeletal Maturity SystemLori A Dolan, Stuart L Weinstein, Mark F Abel, et al.
Journal of Medical Genetics|April 30, 2025
Rare missense variants in <i>FNDC1</i> are associated with severe adolescent idiopathic scoliosisWu-Lin Charng, Gabe Haller, Julia Whittle, et al.
Human Molecular Genetics|October 26, 2020
Genetic association and characterization of FSTL5 in isolated clubfootAnas M Khanshour, Yared H Kidane, Julia Kozlitina, et al.
Journal of Medical Genetics|February 27, 2019
Distal chromosome 16p11.2 duplications containing <i>SH2B1</i> in patients with scoliosisBrooke Sadler, Gabe Haller, Lilian Antunes, et al.
Human Molecular Genetics|January 11, 2011
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSwarkar Sharma, Xiaochong Gao, Douglas Londono, et al.
Pageof 22

Showing results (201-210 of 218) with videos related to

Sort By:
Pageof 22
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.
Human Molecular Genetics|January 5, 2010
Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1Christina A Gurnett, David M Desruisseau, Kevin McCall, et al.
Biology of Reproduction|July 16, 2016
Identification of Beef Heifers with Superior Uterine Capacity for PregnancyThomas W Geary, Gregory W Burns, Joao G N Moraes, et al.
Nature Reviews. Disease Primers|May 19, 2016
Adolescent idiopathic scoliosisJack C Cheng, René M Castelein, Winnie C Chu, et al.
G3 (Bethesda, Md.)|December 16, 2014
Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosisErin E Baschal, Cambria I Wethey, Kandice Swindle, et al.
Spine Deformity|November 17, 2019
Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST): Development and Validation of a Prognostic Model in Untreated Adolescent Idiopathic Scoliosis Using the Simplified Skeletal Maturity SystemLori A Dolan, Stuart L Weinstein, Mark F Abel, et al.
Journal of Medical Genetics|April 30, 2025
Rare missense variants in <i>FNDC1</i> are associated with severe adolescent idiopathic scoliosisWu-Lin Charng, Gabe Haller, Julia Whittle, et al.
Human Molecular Genetics|October 26, 2020
Genetic association and characterization of FSTL5 in isolated clubfootAnas M Khanshour, Yared H Kidane, Julia Kozlitina, et al.
Journal of Medical Genetics|February 27, 2019
Distal chromosome 16p11.2 duplications containing <i>SH2B1</i> in patients with scoliosisBrooke Sadler, Gabe Haller, Lilian Antunes, et al.
Human Molecular Genetics|January 11, 2011
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSwarkar Sharma, Xiaochong Gao, Douglas Londono, et al.
Pageof 22