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S L Sawyer

Showing results (1-10 of 8) with videos related to

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Current Oncology (Toronto, Ont.)|December 23, 2017
Using family history forms in pediatric oncology to identify patients for genetic assessmentA Hamilton, E Smith, J Hamon, et al.
Royal Society Open Science|July 1, 2022
Estimating the effect of non-pharmaceutical interventions on US SARS-CoV-2 infections in the first year of the pandemicN A Duncan, G F L'Her, A G Osborne, et al.
Trends in Genetics : TIG|June 22, 2001
SNP association studies in Alzheimer's disease highlight problems for complex disease analysisT Emahazion, L Feuk, M Jobs, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's diseaseJ A Prince, L Feuk, S L Sawyer, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Clinical Genetics|July 22, 2014
Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective studyD A Dyment, M Tétreault, C L Beaulieu, et al.
Clinical Genetics|October 27, 2015
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Oncology (Toronto, Ont.)|December 23, 2017
Using family history forms in pediatric oncology to identify patients for genetic assessmentA Hamilton, E Smith, J Hamon, et al.
Royal Society Open Science|July 1, 2022
Estimating the effect of non-pharmaceutical interventions on US SARS-CoV-2 infections in the first year of the pandemicN A Duncan, G F L'Her, A G Osborne, et al.
Trends in Genetics : TIG|June 22, 2001
SNP association studies in Alzheimer's disease highlight problems for complex disease analysisT Emahazion, L Feuk, M Jobs, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's diseaseJ A Prince, L Feuk, S L Sawyer, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Clinical Genetics|July 22, 2014
Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective studyD A Dyment, M Tétreault, C L Beaulieu, et al.
Clinical Genetics|October 27, 2015
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Pageof 1