Mireille Cloutier
Ottawa, ON, Canada
Last Updated: 09/26/2026
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Found 9 publications
User evaluation of an implementation toolkit for maternal-newborn care settings.
Journal: JBI evidence implementation
Published: December 02, 2025
FGF14 GAA Intronic Expansion in Unsolved Adult-Onset Ataxia in the Care4Rare Canada Consortium.
Journal: Annals of clinical and translational neurology
Published: October 23, 2024
The diagnostic yield of genetic and metabolic investigations in syndromic and nonsyndromic patients with autism spectrum disorder, global developmental delay, or intellectual disability from a dedicated neurodevelopmental disorders genetics clinic.
Journal: American journal of medical genetics. Part A
Published: March 06, 2024
Genetic and metabolic investigations for individuals with neurodevelopmental disorders: A survey of Canadian geneticists' practices.
Journal: American journal of medical genetics. Part A
Published: October 13, 2020
Lexigene®: An online medical genetics translation tool to facilitate communication.
Journal: Journal of genetic counseling
Published: February 16, 2019
Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis.
Journal: American journal of medical genetics. Part A
Published: October 13, 2018
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 05, 2017
Group genetic counseling: An alternate service delivery model in a high risk prenatal screening population.
Journal: Prenatal diagnosis
Published: January 11, 2017
Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study.
Journal: Fetal diagnosis and therapy
Published: October 18, 2016
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Last Updated: 09/26/2026