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Human Mutation
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July 29, 2022
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorder
Beau D E Janssen, Marie-Jose H van den Boogaard, Klaske Lichtenbelt, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
September 5, 2001
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group
D M Green, N E Breslow, J B Beckwith, et al.
International Journal of Molecular Sciences
|
December 11, 2022
Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear Palsy
Fabio A Simoes, Greig Joilin, Oliver Peters, et al.
Nature Genetics
|
March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver disease
Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Addiction (Abingdon, England)
|
May 31, 2016
Improving the delivery of brief interventions for heavy drinking in primary health care: outcome results of the Optimizing Delivery of Health Care Intervention (ODHIN) five-country cluster randomized factorial trial
Peter Anderson, Preben Bendtsen, Fredrik Spak, et al.
Plos Biology
|
September 14, 2007
High-throughput in vivo analysis of gene expression in Caenorhabditis elegans
Rebecca Hunt-Newbury, Ryan Viveiros, Robert Johnsen, et al.
Implementation Science : IS
|
July 17, 2016
Impact of primary healthcare providers' initial role security and therapeutic commitment on implementing brief interventions in managing risky alcohol consumption: a cluster randomised factorial trial
M Keurhorst, P Anderson, M Heinen, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2016
Clinical and genetic aspects of KBG syndrome
Karen Low, Tazeen Ashraf, Natalie Canham, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new cases
Lucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Plos Genetics
|
March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment
Pía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Page
of 83
Search research articles
Search
Showing results (761-770 of 826) with videos related to
Sort By:
Page
of 83
Human Mutation
|
July 29, 2022
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorder
Beau D E Janssen, Marie-Jose H van den Boogaard, Klaske Lichtenbelt, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
September 5, 2001
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group
D M Green, N E Breslow, J B Beckwith, et al.
International Journal of Molecular Sciences
|
December 11, 2022
Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear Palsy
Fabio A Simoes, Greig Joilin, Oliver Peters, et al.
Nature Genetics
|
March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver disease
Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Addiction (Abingdon, England)
|
May 31, 2016
Improving the delivery of brief interventions for heavy drinking in primary health care: outcome results of the Optimizing Delivery of Health Care Intervention (ODHIN) five-country cluster randomized factorial trial
Peter Anderson, Preben Bendtsen, Fredrik Spak, et al.
Plos Biology
|
September 14, 2007
High-throughput in vivo analysis of gene expression in Caenorhabditis elegans
Rebecca Hunt-Newbury, Ryan Viveiros, Robert Johnsen, et al.
Implementation Science : IS
|
July 17, 2016
Impact of primary healthcare providers' initial role security and therapeutic commitment on implementing brief interventions in managing risky alcohol consumption: a cluster randomised factorial trial
M Keurhorst, P Anderson, M Heinen, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2016
Clinical and genetic aspects of KBG syndrome
Karen Low, Tazeen Ashraf, Natalie Canham, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new cases
Lucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Plos Genetics
|
March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment
Pía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Page
of 83