Linlea Armstrong

Clinical Associate Professor

The University of British Columbia

Research Interests

Explore related searches

Contact this professor

Google Scholar

Articles (15)

Collaborators (14)

M. E. Suzanne Lewis

Hui-Lin Chin

Assistant Professor

National University of Singapore (NUS)

Sally Ann Lynch

Frederick K. Kozak

Clinical Professor

The University of British Columbia

Rebecca Deyell

Clinical Associate Professor

The University of British Columbia

Lorne Clarke

The University of British Columbia

James Whitlock

Division Head

Hospital for Sick Children

Karen Gripp

Nemours Children's Health System

UNITED STATES

William Gibson

BC Children's Hospital

Ingrid Price

Associate Professor of Teaching

The University of British Columbia

Jan Friedman

The University of British Columbia

Cornelius F. Boerkoel

Mariko Nakano-Okuno

The University of Alabama

UNITED STATES

Millan S. Patel

Linlea Armstrong

Research Interests

Explore related searches

Contact this professor

Articles (15)

Collaborators (14)

M. E. Suzanne Lewis

Hui-Lin Chin

Sally Ann Lynch

Frederick K. Kozak

Rebecca Deyell

Lorne Clarke

James Whitlock

Karen Gripp

William Gibson

Ingrid Price

Jan Friedman

Cornelius F. Boerkoel

Mariko Nakano-Okuno

Millan S. Patel

How do I reach out?

Meet Kite AI

Linlea Armstrong

Research Interests

Explore related searches

Contact this professor

Articles (15)

Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

The practice of genomic medicine: A delineation of the process and its governing principles

Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes

Characterization of Switch/Sucrose Nonfermenting Complex Proteins and Nestin Expression in a Cohort of Pediatric Central Nervous System Tumors

Impact of Variation in Practice in the Prenatal Reporting of Variants of Uncertain Significance by Commercial Laboratories: Need for Greater Adherence to Published Guidelines

The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice

Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study

Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines

Primary cutaneous follicle center lymphoma of the medial canthus of the eye in an 11-year old

Crizotinib response in a neuroblastoma patient with a constitutional mosaic anaplastic lymphoma kinase I1170N‐activating mutation

Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation

Coaching the coaches: Employing role modeling and coaching as a faculty development strategy

Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes

Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications

Collaborators (14)

M. E. Suzanne Lewis

Hui-Lin Chin

Sally Ann Lynch

Frederick K. Kozak

Rebecca Deyell

Lorne Clarke

James Whitlock

Karen Gripp

William Gibson

Ingrid Price

Jan Friedman

Cornelius F. Boerkoel

Mariko Nakano-Okuno

Millan S. Patel

How do I reach out?

Meet Kite AI