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Pediatric Research
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July 23, 2025
Multiple domains of efficacy define the utility of genetic testing
Catherine Marx, Amy Y Pan, Robin Z Hayeems, et al.
Paediatrics & Child Health
|
March 11, 2022
Understanding genetic variants of uncertain significance
Alyssa C M Joynt, Michelle M Axford, Lauren Chad, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
October 26, 2021
Genome sequencing as a diagnostic test
Gregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
The Lancet. Psychiatry
|
September 12, 2015
Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia
Kate Baker, Gregory Costain, Wai Lun Alan Fung, et al.
American Journal of Medical Genetics. Part A
|
February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype
Gregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
Journal of Medical Genetics
|
November 5, 2011
Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions
Gregory Costain, Eva W C Chow, Candice K Silversides, et al.
Schizophrenia Bulletin
|
October 30, 2012
Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age
Gregory Costain, Mary Jane Esplen, Brenda Toner, et al.
Ophthalmic Genetics
|
May 14, 2021
Novel heterozygous variants in <i>PXDN</i> cause different anterior segment dysgenesis phenotypes in monozygotic twins
Angela Y Zhu, Gregory Costain, Cheryl Cytrynbaum, et al.
International Journal of Cardiology
|
November 10, 2015
Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease
Gregory Costain, S Lucy Roche, Stephen W Scherer, et al.
Clinical Pharmacology and Therapeutics
|
April 29, 2025
Impaired Drug Metabolism Caused by Compound Heterozygous Loss-of-Function Variants in CYP3A4: A Case Report
Han Byul Kang, Iris Cohn, Sanjay Mahant, et al.
Page
of 15
Search research articles
Search
Showing results (21-30 of 144) with videos related to
Sort By:
Page
of 15
Pediatric Research
|
July 23, 2025
Multiple domains of efficacy define the utility of genetic testing
Catherine Marx, Amy Y Pan, Robin Z Hayeems, et al.
Paediatrics & Child Health
|
March 11, 2022
Understanding genetic variants of uncertain significance
Alyssa C M Joynt, Michelle M Axford, Lauren Chad, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
October 26, 2021
Genome sequencing as a diagnostic test
Gregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
The Lancet. Psychiatry
|
September 12, 2015
Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia
Kate Baker, Gregory Costain, Wai Lun Alan Fung, et al.
American Journal of Medical Genetics. Part A
|
February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype
Gregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
Journal of Medical Genetics
|
November 5, 2011
Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions
Gregory Costain, Eva W C Chow, Candice K Silversides, et al.
Schizophrenia Bulletin
|
October 30, 2012
Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age
Gregory Costain, Mary Jane Esplen, Brenda Toner, et al.
Ophthalmic Genetics
|
May 14, 2021
Novel heterozygous variants in <i>PXDN</i> cause different anterior segment dysgenesis phenotypes in monozygotic twins
Angela Y Zhu, Gregory Costain, Cheryl Cytrynbaum, et al.
International Journal of Cardiology
|
November 10, 2015
Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease
Gregory Costain, S Lucy Roche, Stephen W Scherer, et al.
Clinical Pharmacology and Therapeutics
|
April 29, 2025
Impaired Drug Metabolism Caused by Compound Heterozygous Loss-of-Function Variants in CYP3A4: A Case Report
Han Byul Kang, Iris Cohn, Sanjay Mahant, et al.
Page
of 15