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Showing results (211-220 of 218) with videos related to

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Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Spine|November 23, 2023
BrAIST-Calc: Prediction of Individualized Benefit From Bracing for Adolescent Idiopathic ScoliosisLori A Dolan, Stuart L Weinstein, Matthew B Dobbs, et al.
Human Molecular Genetics|January 9, 2009
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypesMika Asai-Coakwell, Curtis R French, Ming Ye, et al.
Cell|March 15, 2020
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer VariantsEvgeny Z Kvon, Yiwen Zhu, Guy Kelman, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|March 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|February 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Pageof 22

Showing results (211-220 of 218) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 218 results.
Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Spine|November 23, 2023
BrAIST-Calc: Prediction of Individualized Benefit From Bracing for Adolescent Idiopathic ScoliosisLori A Dolan, Stuart L Weinstein, Matthew B Dobbs, et al.
Human Molecular Genetics|January 9, 2009
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypesMika Asai-Coakwell, Curtis R French, Ming Ye, et al.
Cell|March 15, 2020
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer VariantsEvgeny Z Kvon, Yiwen Zhu, Guy Kelman, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|March 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|February 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Pageof 22