Kathy Chun
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 10 publications
Two cases of mosaic germline SVA insertions in SMARCB1: implications for rhabdoid tumour predisposition diagnosis.
Journal: NPJ genomic medicine
Published: December 24, 2025
De novo triplication at 1p36.23p36.22 further refines the dosage sensitive region of overlap in Setleis syndrome (focal facial dermal dysplasia type III).
Journal: American journal of medical genetics. Part A
Published: November 13, 2022
Development of a comprehensive approach to adult hereditary cancer testing in Ontario.
Journal: Journal of medical genetics
Published: September 16, 2022
The Clinical Landscape of NRAS- mutated Juvenile Myelomonocytic Leukemia-like Myeloproliferation Includes Children With Costello Syndrome.
Journal: Journal of pediatric hematology/oncology
Published: March 09, 2022
Building the What Comes Next Cohort for BRCA1 and BRCA2 testing: a descriptive analysis.
Journal: CMAJ open
Published: December 06, 2021
Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories.
Journal: Prenatal diagnosis
Published: June 29, 2020
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 06, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026