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Showing results (861-870 of 915) with videos related to

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Annals of the Rheumatic Diseases|December 9, 2016
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implicationsMichael J Ombrello, Victoria L Arthur, Elaine F Remmers, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 2015
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritisMichael J Ombrello, Elaine F Remmers, Ioanna Tachmazidou, et al.
The Journal of Clinical Investigation|May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.
European Journal of Human Genetics : EJHG|August 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathologyHenry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
BMC Genomic Data|May 2, 2023
HostSeq: a Canadian whole genome sequencing and clinical data resourceS Yoo, E Garg, L T Elliott, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
Pageof 92

Showing results (861-870 of 915) with videos related to

Sort By:
Pageof 92
Annals of the Rheumatic Diseases|December 9, 2016
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implicationsMichael J Ombrello, Victoria L Arthur, Elaine F Remmers, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 2015
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritisMichael J Ombrello, Elaine F Remmers, Ioanna Tachmazidou, et al.
The Journal of Clinical Investigation|May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.
European Journal of Human Genetics : EJHG|August 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathologyHenry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
BMC Genomic Data|May 2, 2023
HostSeq: a Canadian whole genome sequencing and clinical data resourceS Yoo, E Garg, L T Elliott, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
Pageof 92