• About Us
  • Contact Us
  • Sitemap
  • Permissions
  • Disclaimer
  • Connect

  • Point of Care Tools
    • Cancer genomics
      • BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Syndrome
      • General Hereditary Cancer Syndrome Triage Tool
      • Lynch Syndrome
      • Renal Cell Cancers
    • Cardiogenomics
      • Factor V Leiden
      • Familial hypercholesterolemia
      • Hypertrophic Cardiomyopathy
      • Long QT syndrome
    • General genomics
      • Family History
      • Family history red flags
      • Hereditary Hemochromatosis
    • Neurogenomics
      • Autism spectrum disorder
      • Epilepsy
    • Preconception and prenatal genomics
      • Carrier Screening in Canada
      • Expanded Carrier Screening
      • [A guide to understanding] Prenatal Screening
  • Educational Resources
    • Cancer Genomics
      • BRCA1/BRCA2 Hereditary Breast and Ovarian Cancer Syndrome
      • Lynch Syndrome (Hereditary colorectal cancer)
    • Cardiogenomics
      • Factor V Leiden
      • Familial hypercholesterolemia
      • Hypertrophic cardiomyopathy
      • Long QT syndrome 
    • General Genomics
      • Basic genomic resources
      • Hearing loss (the genetics of)
      • Hereditary Hemochromatosis
      • Schizophrenia
      • Type 2 Diabetes
    • Neurogenomics
      • Alzheimer disease
      • Autism spectrum disorder (ASD)
      • Epilepsy
      • Huntington disease
      • Multiple sclerosis
    • Pharmacogenomics
      • Codeine and breastfeeding
      • Additional resources
    • Prenatal and Preconception Genomics
      • Consanguinity
      • Carrier screening in Canada
      • Expanded carrier screening
      • Non-invasive prenatal testing (NIPT)
      • Prenatal Screening
    • Technologies
      • Chromosomal microarray
      • Chromosomal microarray – PRENATAL
      • Direct-to-consumer genetic testing
      • Expanded carrier screening
      • Non-invasive prenatal testing (NIPT)
      • Prenatal Screening
      • Whole Exome and Genome Sequencing
    • Basic Genomic Resources
    • Glossary
    • Additional Resources
  • PowerPoint Seminars
    • Cardiogenomics
    • Prenatal and Preconception Genetics
    • Pediatric Genetics
    • Adult Genetics
    • General Genetic Counselling
  • Genetics Centres
    • Canada
      • Clinics
      • Laboratories
    • Outside Canada
  • Public Resources
    • General Resources
    • Prenatal and Preconception Genetics
      • Guide to understanding prenatal screening tests
    • Newborn Genetics
    • Adult Genetics
  • News & Events

Not-for-profit genetics and genomics education for non-genetics health professionals

#UntanglingTheHelix

CanImpact Alberta

CanImpact Alberta Personal Cancer Genomic Medicine Resource Toolkit

CanImpact logo AB

  • GEC-KO on the run
    • [Prenatal] Chromosomal Microarray
    • Alzheimer disease
    • Autism spectrum disorder
    • Colorectal Cancer – Lynch syndrome
    • Consanguinity
    • Diabetes Type 2
    • Direct-to-Consumer Genetic Testing
    • Factor V Leiden – Inherited Thrombophilia
    • Familial hypercholesterolemia
    • Genetics of epilepsy
    • Hereditary Breast and Ovarian Cancer (BRCA1/BRCA2)
    • Hereditary Hemochromatosis
    • Huntington Disease
    • Hypertrophic cardiomyopathy
    • Long QT syndrome
    • Microarray
    • Multiple Sclerosis
    • Non-invasive prenatal testing
    • Pharmacogenomics – Codeine and Breastfeeding
    • Schizophrenia
  • GEC-KO Messengers
    • Autism spectrum disorder
    • Consanguinity
    • Direct-to-consumer genetic testing
    • Factor V Leiden – Inherited Thrombophilia
    • Familial hypercholesterolemia
    • Genetics of epilepsy
    • Hereditary Breast and Ovarian Cancer (BRCA1/BRCA2)
    • Hereditary Hemochromatosis
    • Lynch Syndrome
    • Multiple Sclerosis
  • Cancer Genomics
    • BRCA1/BRCA2 Hereditary Breast and Ovarian Cancer Syndrome
    • Lynch Syndrome (Hereditary colorectal cancer)
  • Other GEC-KO Resources
  • Cardiogenomics
    • Factor V Leiden
    • Familial hypercholesterolemia
    • Hypertrophic cardiomyopathy
    • Long QT syndrome 
  • General Genomics
    • Basic genomic resources
    • Hearing loss (the genetics of)
    • Hereditary Hemochromatosis
    • Schizophrenia
    • Type 2 Diabetes
  • Basic Genomic Resources
  • Neurogenomics
    • Alzheimer disease
    • Autism spectrum disorder (ASD)
    • Epilepsy
    • Huntington disease
    • Multiple sclerosis
  • Glossary
  • Pharmacogenomics
    • Additional resources
    • Codeine and breastfeeding
  • Prenatal and Preconception Genomics
    • [A Guide to Understanding] Prenatal Screening
    • Carrier screening in Canada
    • Consanguinity
    • Non-invasive prenatal testing (NIPT)
  • Additional Resources
  • CanImpact Alberta
  • CanImpact Ontario
  • Technologies
    • [A Guide to Understanding] Prenatal Screening (technology)
    • Chromosomal microarray
    • Chromosomal microarray – PRENATAL
    • Direct-to-consumer genetic testing
    • Expanded carrier screening
    • Non-invasive prenatal testing (NIPT)
    • Whole Exome and Genome Sequencing
    • Whole Exome and Genome Sequencing
  • About Us
  • Contact Us
  • Sitemap
  • Permissions
  • Disclaimer
  • Connect

Tweets

ECHO Epilepsy Ontario
6 Feb
ECHO Epilepsy Ontario
@ECHOEpilepsy

Community Neurologists & #PrimaryCare providers - join Dr. Kevin Jones, paediatric neurologist @mch_childrens and our #EpilepsyGenetics community for "Epilepsy Gene Panel Selection, Pt.2" 🔎Case discussion follows. Feb. 9 | 12-1pm REGISTER➡️oen.echoontario.ca/genetics-a… #MedEd #CME pic.twitter.com/J0rL4CzAbH

Retweeted by GECKORetweeted by GECKO
Expand reply reply retweet retweet favorite favorite
Genetics in Medicine
3 Feb
Genetics in Medicine
@GIMJournal

Genetics in Medicine's February issue is now available online gimjournal.org/current. Register here for monthly electronic Table of Contents: bit.ly/Register_GIM_E… pic.twitter.com/kYr5gy16ul

Retweeted by GECKORetweeted by GECKO
Expand reply reply retweet retweet favorite favorite
Sickle Cell Awareness Group of Ontario (SCAGO)
3 Feb
Sickle Cell Awareness Group of Ontario (SCAGO)
@SCAGOSCD

We are delighted to announce that we are back with Hope Gala & Awards this year, we are inviting you to put on your party wear and help reach vital funds for sickle cell disease. GET YOUR TICKETS NOW ow.ly/aOCu50MCs5B pic.twitter.com/xzLgKUqXoO

Retweeted by GECKORetweeted by GECKO
Expand reply reply retweet retweet favorite favorite
ECHO Epilepsy Ontario
3 Feb
ECHO Epilepsy Ontario
@ECHOEpilepsy

*date correction #PrimaryCare Providers, join our #PedsEpilepsy community for a talk by Dr. Elizabeth Donner's on managing antiseizure medications: "Selecting Appropriate AEDs, Managing Side Effects" Monday, Feb. 6 | 12-1pm Register➡️oen.echoontario.ca/programs/c… #MedEd twitter.com/ECHOEpilepsy/s… pic.twitter.com/YiFBJJZvpC

Retweeted by GECKORetweeted by GECKO
Expand reply reply retweet retweet favorite favorite
GECKO
3 Feb
GECKO
@GECKOgenetics

Have your say and help improve prenatal care! twitter.com/OntarioPSO/sta…

Expand reply reply retweet retweet favorite favorite
  • Twitter
© 2020. GEC-KO | Genetics Education Canada - Knowledge Organization
Scroll
×

Subscribe


Subscribe to our updates and be the first to know about new GEC-KO resources.