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The British Journal of General Practice : the Journal of the Royal College of General Practitioners
|
April 1, 1996
Pilot study of the acceptability of cystic fibrosis carrier testing during routine antenatal consultations in general practice
H Harris, D Scotcher, N Hartley, et al.
Veterinary Research
|
January 25, 2014
Frequency of IFNγ-producing T cells correlates with seroreactivity and activated T cells during canine Trypanosoma cruzi infection
Ashley N Hartley, Gretchen Cooley, Sarah Gwyn, et al.
Case Reports in Pediatrics
|
August 29, 2012
Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia
Jessica N Hartley, Frances A Booth, Marc R Del Bigio, et al.
Clinical Orthopaedics and Related Research
|
May 1, 1978
Efficacy of graded-compression antiembolism stockings in patients undergoing total hip arthroplasty
R W Barnes, R A Brand, W Clarke, et al.
Plant, Cell & Environment
|
April 25, 2017
Genome-wide association studies to identify rice salt-tolerance markers
Juan Patishtan, Tom N Hartley, Raquel Fonseca de Carvalho, et al.
Journal of Telemedicine and Telecare
|
September 23, 2015
Exploring the predictors of home telehealth uptake by elderly Australian healthcare consumers
T G Russell, N Gillespie, N Hartley, et al.
Journal of Genetic Counseling
|
April 28, 2023
Insights into genetic assistant practice and the workforce in North America
Angela Krutish, Xiao-Qing Liu, Christine Kelly, et al.
The Journal of Small Animal Practice
|
April 23, 2024
The epidemiology of tick infestation in dog breeds in the UK
D G O'Neill, R Komutrattananon, D B Church, et al.
Diseases of the Colon and Rectum
|
June 1, 1996
Comparison of individual surgeon's performance. Risk-adjusted analysis with POSSUM scoring system
P M Sagar, M N Hartley, J MacFie, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2018
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families
Jessica N Hartley, Louise R Simard, Valentina Ly, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 65) with videos related to
Sort By:
Page
of 7
The British Journal of General Practice : the Journal of the Royal College of General Practitioners
|
April 1, 1996
Pilot study of the acceptability of cystic fibrosis carrier testing during routine antenatal consultations in general practice
H Harris, D Scotcher, N Hartley, et al.
Veterinary Research
|
January 25, 2014
Frequency of IFNγ-producing T cells correlates with seroreactivity and activated T cells during canine Trypanosoma cruzi infection
Ashley N Hartley, Gretchen Cooley, Sarah Gwyn, et al.
Case Reports in Pediatrics
|
August 29, 2012
Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia
Jessica N Hartley, Frances A Booth, Marc R Del Bigio, et al.
Clinical Orthopaedics and Related Research
|
May 1, 1978
Efficacy of graded-compression antiembolism stockings in patients undergoing total hip arthroplasty
R W Barnes, R A Brand, W Clarke, et al.
Plant, Cell & Environment
|
April 25, 2017
Genome-wide association studies to identify rice salt-tolerance markers
Juan Patishtan, Tom N Hartley, Raquel Fonseca de Carvalho, et al.
Journal of Telemedicine and Telecare
|
September 23, 2015
Exploring the predictors of home telehealth uptake by elderly Australian healthcare consumers
T G Russell, N Gillespie, N Hartley, et al.
Journal of Genetic Counseling
|
April 28, 2023
Insights into genetic assistant practice and the workforce in North America
Angela Krutish, Xiao-Qing Liu, Christine Kelly, et al.
The Journal of Small Animal Practice
|
April 23, 2024
The epidemiology of tick infestation in dog breeds in the UK
D G O'Neill, R Komutrattananon, D B Church, et al.
Diseases of the Colon and Rectum
|
June 1, 1996
Comparison of individual surgeon's performance. Risk-adjusted analysis with POSSUM scoring system
P M Sagar, M N Hartley, J MacFie, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2018
A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families
Jessica N Hartley, Louise R Simard, Valentina Ly, et al.
Page
of 7