Breanne Dale

Hamilton, ON, Canada

Last Updated: 09/26/2026

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Found 8 publications

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Journal: European journal of human genetics : EJHG

Published: April 02, 2026

DEGS1-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of Literature.

DEGS1-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of Literature.

Journal: Neurology. Genetics

Published: March 30, 2025

Severe Epilepsy in an Individual With a TSC2 R905Q Variant Prompting Late Diagnosis in Affected Family Members.

Severe Epilepsy in an Individual With a TSC2 R905Q Variant Prompting Late Diagnosis in Affected Family Members.

Journal: Pediatric neurology

Published: July 25, 2024

Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Journal: European journal of human genetics : EJHG

Published: June 23, 2024

Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Journal: European journal of human genetics : EJHG

Published: June 23, 2024

Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant.

Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant.

Journal: BMJ case reports

Published: January 03, 2023

Pathogenic DNM1 Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case Report.

Pathogenic DNM1 Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case Report.

Journal: Neurology. Genetics

Published: March 24, 2021

Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage.

Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage.

Journal: NPJ genomic medicine

Published: November 22, 2016

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Last Updated: 09/26/2026