Search research articles
Contact Us
Filters
Showing results (1-10 of 34) with videos related to
Page
of 4
Sort By:
The Application of Clinical Genetics
|
June 19, 2013
Alpha1-antitrypsin deficiency: a clinical-genetic overview
Raja T Abboud, Tanya N Nelson, Benjamin Jung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2012
Uniparental disomy: can SNP array data be used for diagnosis?
Tracy Tucker, Kamilla Schlade-Bartusiak, Patrice Eydoux, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Performance of a Three-Tier (IRT-DNA-IRT) Cystic Fibrosis Screening Algorithm in British Columbia
Graham Sinclair, Vanessa McMahon, Amy Schellenberg, et al.
American Journal of Medical Genetics. Part A
|
June 27, 2007
Renal-hepatic-pancreatic dysplasia: an autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1-p12
Kasmintan A Schrader, Tanya N Nelson, Deborah E McFadden, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 11, 2009
A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction
Michelle K Demos, Vincenzo Macri, Kevin Farrell, et al.
Clinical Dysmorphology
|
December 5, 2015
Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features
Tracy Tucker, Michelle Steinraths, Tracey Oh, et al.
Journal of Medical Genetics
|
August 21, 2017
Choosing Wisely Canada: The Canadian College of Medical Geneticists' (CCMG) list of five items physicians and patients should question
Elaine Goh, Andrea Guerin, Joanna Lazier, et al.
Journal of Medical Genetics
|
July 14, 2019
CCMG practice guideline: laboratory guidelines for next-generation sequencing
Stacey Hume, Tanya N Nelson, Marsha Speevak, et al.
Journal of Medical Genetics
|
August 24, 2025
Reproductive carrier screening for genetic disorders: position statement of the Canadian College of Medical Geneticists
Ritu B Aul, Karen Elizabeth Canales, Isabelle De Bie, 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.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
The Application of Clinical Genetics
|
June 19, 2013
Alpha1-antitrypsin deficiency: a clinical-genetic overview
Raja T Abboud, Tanya N Nelson, Benjamin Jung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2012
Uniparental disomy: can SNP array data be used for diagnosis?
Tracy Tucker, Kamilla Schlade-Bartusiak, Patrice Eydoux, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Performance of a Three-Tier (IRT-DNA-IRT) Cystic Fibrosis Screening Algorithm in British Columbia
Graham Sinclair, Vanessa McMahon, Amy Schellenberg, et al.
American Journal of Medical Genetics. Part A
|
June 27, 2007
Renal-hepatic-pancreatic dysplasia: an autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1-p12
Kasmintan A Schrader, Tanya N Nelson, Deborah E McFadden, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 11, 2009
A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction
Michelle K Demos, Vincenzo Macri, Kevin Farrell, et al.
Clinical Dysmorphology
|
December 5, 2015
Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features
Tracy Tucker, Michelle Steinraths, Tracey Oh, et al.
Journal of Medical Genetics
|
August 21, 2017
Choosing Wisely Canada: The Canadian College of Medical Geneticists' (CCMG) list of five items physicians and patients should question
Elaine Goh, Andrea Guerin, Joanna Lazier, et al.
Journal of Medical Genetics
|
July 14, 2019
CCMG practice guideline: laboratory guidelines for next-generation sequencing
Stacey Hume, Tanya N Nelson, Marsha Speevak, et al.
Journal of Medical Genetics
|
August 24, 2025
Reproductive carrier screening for genetic disorders: position statement of the Canadian College of Medical Geneticists
Ritu B Aul, Karen Elizabeth Canales, Isabelle De Bie, 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.
Page
of 4