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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 30, 2019
The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders
Nick Dragojlovic, Clara D M van Karnebeek, Aisha Ghani, et al.
Molecular Genetics & Genomic Medicine
|
June 1, 2018
The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia
Alison M Elliott, Christèle du Souich, Shelin Adam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2024
Where there is no genetic counselor: An online decision-aid supports the majority of parents' diagnostic genomic testing choices for their children
Patricia Birch, Rhea Beauchesne, Nick Bansback, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology
|
December 6, 2014
Exposure-based validation list for developmental toxicity screening assays
George P Daston, Bruce K Beyer, Edward W Carney, et al.
Plos One
|
May 24, 2011
The sensitivity of massively parallel sequencing for detecting candidate infectious agents associated with human tissue
Richard A Moore, René L Warren, J Douglas Freeman, et al.
Obstetrics and Gynecology
|
November 22, 2014
Management of multiple sclerosis during pregnancy and the reproductive years: a systematic review
Riley Bove, Sura Alwan, Jan M Friedman, et al.
Journal of Telemedicine and Telecare
|
January 20, 2021
Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES Study
Alison M Elliott, Nick Dragojlovic, Teresa Campbell, et al.
Health Policy (Amsterdam, Netherlands)
|
May 8, 2021
Utilization and uptake of clinical genetics services in high-income countries: A scoping review
Nick Dragojlovic, Nicola Kopac, Kennedy Borle, et al.
Schizophrenia Research
|
November 26, 2019
Atypical antipsychotic use during pregnancy and birth defect risk: National Birth Defects Prevention Study, 1997-2011
Kayla N Anderson, Elizabeth C Ailes, Jennifer N Lind, et al.
European Journal of Medical Genetics
|
April 18, 2017
A case of splenomegaly in CBL syndrome
Rachel R Coe, Margaret L McKinnon, Maja Tarailo-Graovac, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 165) with videos related to
Sort By:
Page
of 17
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 30, 2019
The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders
Nick Dragojlovic, Clara D M van Karnebeek, Aisha Ghani, et al.
Molecular Genetics & Genomic Medicine
|
June 1, 2018
The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia
Alison M Elliott, Christèle du Souich, Shelin Adam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 3, 2024
Where there is no genetic counselor: An online decision-aid supports the majority of parents' diagnostic genomic testing choices for their children
Patricia Birch, Rhea Beauchesne, Nick Bansback, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology
|
December 6, 2014
Exposure-based validation list for developmental toxicity screening assays
George P Daston, Bruce K Beyer, Edward W Carney, et al.
Plos One
|
May 24, 2011
The sensitivity of massively parallel sequencing for detecting candidate infectious agents associated with human tissue
Richard A Moore, René L Warren, J Douglas Freeman, et al.
Obstetrics and Gynecology
|
November 22, 2014
Management of multiple sclerosis during pregnancy and the reproductive years: a systematic review
Riley Bove, Sura Alwan, Jan M Friedman, et al.
Journal of Telemedicine and Telecare
|
January 20, 2021
Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES Study
Alison M Elliott, Nick Dragojlovic, Teresa Campbell, et al.
Health Policy (Amsterdam, Netherlands)
|
May 8, 2021
Utilization and uptake of clinical genetics services in high-income countries: A scoping review
Nick Dragojlovic, Nicola Kopac, Kennedy Borle, et al.
Schizophrenia Research
|
November 26, 2019
Atypical antipsychotic use during pregnancy and birth defect risk: National Birth Defects Prevention Study, 1997-2011
Kayla N Anderson, Elizabeth C Ailes, Jennifer N Lind, et al.
European Journal of Medical Genetics
|
April 18, 2017
A case of splenomegaly in CBL syndrome
Rachel R Coe, Margaret L McKinnon, Maja Tarailo-Graovac, et al.
Page
of 17