Search research articles
Contact Us
Filters
Showing results (621-630 of 672) with videos related to
Page
of 68
Sort By:
European Heart Journal
|
July 11, 2023
Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy
Mona Allouba, Roddy Walsh, Alaa Afify, et al.
International Journal of Audiology
|
August 30, 2006
Self-reported benefits from successive bilateral cochlear implantation in post-lingually deafened adults: randomised controlled trial
A Quentin Summerfield, G R Barton, J Toner, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
April 30, 2026
Reduced Skeletal Muscle Perfusion Accompanies Skeletal Muscle Atrophy After Severe Spinal Cord Injury
Zachary S Clayton, Branden L Nguyen, Hui Jean Kok, et al.
Human Molecular Genetics
|
December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice
Yaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
BMC Health Services Research
|
March 2, 2011
Evaluation of stroke services in Anglia Stroke Clinical Network to examine the variation in acute services and stroke outcomes
Phyo K Myint, John F Potter, Gill M Price, et al.
American Journal of Human Genetics
|
January 5, 2019
Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture
Nicola Whiffin, Angharad M Roberts, Eric Minikel, et al.
Health Technology Assessment (Winchester, England)
|
May 9, 2014
Rehabilitation aimed at improving outdoor mobility for people after stroke: a multicentre randomised controlled study (the Getting out of the House Study)
Philippa A Logan, Sarah Armstrong, Tony J Avery, et al.
Nature Communications
|
May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals
Nicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature Communications
|
February 3, 2021
Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals
Nicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Circulation. Genomic and Precision Medicine
|
August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant Cardiomyopathy
Parth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Page
of 68
Search research articles
Search
Showing results (621-630 of 672) with videos related to
Sort By:
Page
of 68
European Heart Journal
|
July 11, 2023
Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy
Mona Allouba, Roddy Walsh, Alaa Afify, et al.
International Journal of Audiology
|
August 30, 2006
Self-reported benefits from successive bilateral cochlear implantation in post-lingually deafened adults: randomised controlled trial
A Quentin Summerfield, G R Barton, J Toner, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
April 30, 2026
Reduced Skeletal Muscle Perfusion Accompanies Skeletal Muscle Atrophy After Severe Spinal Cord Injury
Zachary S Clayton, Branden L Nguyen, Hui Jean Kok, et al.
Human Molecular Genetics
|
December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice
Yaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
BMC Health Services Research
|
March 2, 2011
Evaluation of stroke services in Anglia Stroke Clinical Network to examine the variation in acute services and stroke outcomes
Phyo K Myint, John F Potter, Gill M Price, et al.
American Journal of Human Genetics
|
January 5, 2019
Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture
Nicola Whiffin, Angharad M Roberts, Eric Minikel, et al.
Health Technology Assessment (Winchester, England)
|
May 9, 2014
Rehabilitation aimed at improving outdoor mobility for people after stroke: a multicentre randomised controlled study (the Getting out of the House Study)
Philippa A Logan, Sarah Armstrong, Tony J Avery, et al.
Nature Communications
|
May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals
Nicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature Communications
|
February 3, 2021
Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals
Nicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Circulation. Genomic and Precision Medicine
|
August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant Cardiomyopathy
Parth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Page
of 68