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The Lancet. Neurology
|
August 18, 2023
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
Alissa M D'Gama, Sarah Mulhern, Beth R Sheidley, et al.
BMJ Open
|
February 23, 2022
Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study
Andrea J Chow, Ryan Iverson, Monica Lamoureux, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Anath C Lionel, Gregory Costain, Nasim Monfared, et al.
NPJ Genomic Medicine
|
June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
Clinical Genetics
|
November 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data
Taila Hartley, Élisabeth Soubry, Meryl Acker, et al.
American Journal of Human Genetics
|
April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
Sarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.
Page
of 11
Search research articles
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Showing results (101-110 of 106) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 106 results.
The Lancet. Neurology
|
August 18, 2023
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
Alissa M D'Gama, Sarah Mulhern, Beth R Sheidley, et al.
BMJ Open
|
February 23, 2022
Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study
Andrea J Chow, Ryan Iverson, Monica Lamoureux, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Anath C Lionel, Gregory Costain, Nasim Monfared, et al.
NPJ Genomic Medicine
|
June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
Clinical Genetics
|
November 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data
Taila Hartley, Élisabeth Soubry, Meryl Acker, et al.
American Journal of Human Genetics
|
April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome
Sarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.
Page
of 11