Skip to main content
McGill University Health Centre

Search

  • Patients and visitors
    • Admitting
    • Appointments
    • Clinical departments and services
    • End-of-life care
    • Family presence and visiting guidelines
    • Indigenous patients
    • Parking
    • Patient partners
    • Plan your stay
    • Telehealth
    • Test centre
    • Users' (Patients') Committee
  • Our hospitals
    • Glen site
    • Montreal Children's Hospital
    • Montreal General Hospital
    • Lachine Hospital and Camille Lefebvre Pavilion (CHSLD)
    • The Neuro (Montreal Neurological Institute-Hospital)
    • Other sites
  • Support services
    • Accessibility
    • Medical records
    • Ombudsman/Complaints Commissioner
    • Patient accounts
    • Patient Support Line
    • Protecting our patients
    • Recalls
    • Resource centres and libraries
    • Spiritual care
  • Food and amenities
    • ATMs
    • Cafeterias
    • Restaurants and retail
    • Wifi
  • Health professionals
    • Health professional information
    • Health Technology Assessment Unit
    • Laboratories
    • Libraries
    • Teaching and education
  • Careers
    • A career at the MUHC
    • Nursing careers
    • Lab careers
    • See our current opportunities
    • How we work together
    • Work-life balance
    • Inter-establishment movement – Santé Québec
  • Search

    Search

    • Internships
    • Donate
    • IMPACT Centre
    • Volunteering
    • Research
    • News
    • Français
  • Welcome to the McGill University Health Centre
  1. Home
  2. Core Molecular Diagnostic Laboratory
  3. Tests
  4. Genetics
About us
Tests
Genetics
Molecular pathology
Requisitions
Contact

Genetics

Explore available genetic tests in our catalogue.

Select a test to view detailed information, including indications, methodology, and interpretation.

  • Alpha-1-antitrypsin deficiency
  • Amyotrophic Lateral Sclerosis
  • Angelman/Prader-Willi syndrome
  • Ashkenazi Jewish Carrier Screening
  • Beta-thalassemia and sickle cell anemia
  • Clouston Syndrome
  • Cystic Fibrosis and CFTR-related Conditions
  • DPYD genotyping
  • Dysbetalipoproteinemia
  • Familial hypercholesterolemia
  • Genotyping of short tandem repeats
  • Hereditary Cancer Predisposition Syndrome Panel
  • Hereditary hemochromatosis
  • Huntington Disease
  • Maternal cell contamination
  • MCAD Deficiency
  • MMACHC-related methylmalonic acidemia and homocystinuria
  • Non-syndromic Hearing Loss Panel (Exome)
  • Pediatric Solid Tumour Predisposition Syndromes (Exome)
  • Phenylalanine hydroxylase deficiency
  • Postnatal Aneuploidy Detection by QF-PCR
  • Prenatal Aneuploidy Detection by QF-PCR
  • Tay-Sachs disease
  • Y-chromosome microdeletion
About the MUHC
  • Corporate leadership
  • MUHC at a glance
  • Vision, mission and values
  • Clinical departments and services
  • Sustainable development
  • Call for public tenders
  • Logibec GCH Espresso
  • MyMUHC/intranet
  • Règlement intérieur de l’établissement de Santé Québec - CUSM/MUHC
  • Laws applicable to Québec health and social services establishments
  • Reports
  • Facebook
  • Twitter
  • Instagram
  • LinkedIn
  • Blue Sky
  • Contact us
  • Media contact
  • Social media and netiquette
  • MUHC Permanent Archives Centre
  • MUHC Publications
  • RBC Art and Heritage Centre
  • McGill University Health Centre
  • Disclaimer
  • Privacy
  • Supplier complaints (AMP)
  • © McGill University Health Centre 2026