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Hywel Williams

Showing results (71-80 of 86) with videos related to

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Trials|January 9, 2020
Trial Forge Guidance 2: how to decide if a further Study Within A Trial (SWAT) is neededShaun Treweek, Simon Bevan, Peter Bower, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's diseasePeter Holmans, Marian Hamshere, Paul Hollingworth, et al.
Trials|June 23, 2012
A multi-centre randomised controlled trial of rehabilitation aimed at improving outdoor mobility for people after stroke: study protocol for a randomised controlled trialPip A Logan, Mat P Leighton, Marion F Walker, et al.
Archives of General Psychiatry|July 7, 2010
Psychosis susceptibility gene ZNF804A and cognitive performance in schizophreniaJames T R Walters, Aiden Corvin, Michael J Owen, et al.
American Journal of Medical Genetics|February 22, 2002
Full genome screen for Alzheimer disease: stage II analysisAmanda Myers, Fabienne Wavrant De-Vrieze, Peter Holmans, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiencyLeyla Akin, Karine Rizzoti, Louise C Gregory, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Allergy|August 1, 2012
Towards global consensus on outcome measures for atopic eczema research: results of the HOME II meetingJochen Schmitt, Phyllis Spuls, Maarten Boers, et al.
Thorax|August 10, 2017
High prevalence of <i>CCDC103</i> p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigationsAmelia Shoemark, Eduardo Moya, Robert A Hirst, et al.
Science (New York, N.Y.)|April 27, 2002
No major schizophrenia locus detected on chromosome 1q in a large multicenter sampleDouglas F Levinson, Peter A Holmans, Claudine Laurent, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Trials|January 9, 2020
Trial Forge Guidance 2: how to decide if a further Study Within A Trial (SWAT) is neededShaun Treweek, Simon Bevan, Peter Bower, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's diseasePeter Holmans, Marian Hamshere, Paul Hollingworth, et al.
Trials|June 23, 2012
A multi-centre randomised controlled trial of rehabilitation aimed at improving outdoor mobility for people after stroke: study protocol for a randomised controlled trialPip A Logan, Mat P Leighton, Marion F Walker, et al.
Archives of General Psychiatry|July 7, 2010
Psychosis susceptibility gene ZNF804A and cognitive performance in schizophreniaJames T R Walters, Aiden Corvin, Michael J Owen, et al.
American Journal of Medical Genetics|February 22, 2002
Full genome screen for Alzheimer disease: stage II analysisAmanda Myers, Fabienne Wavrant De-Vrieze, Peter Holmans, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiencyLeyla Akin, Karine Rizzoti, Louise C Gregory, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Allergy|August 1, 2012
Towards global consensus on outcome measures for atopic eczema research: results of the HOME II meetingJochen Schmitt, Phyllis Spuls, Maarten Boers, et al.
Thorax|August 10, 2017
High prevalence of <i>CCDC103</i> p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigationsAmelia Shoemark, Eduardo Moya, Robert A Hirst, et al.
Science (New York, N.Y.)|April 27, 2002
No major schizophrenia locus detected on chromosome 1q in a large multicenter sampleDouglas F Levinson, Peter A Holmans, Claudine Laurent, et al.
Pageof 9