• 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

Family History App in Personalized Medicine (FHAMe): Diabetes

morrison    1 year ago  

FHAMe Diabetes

1

morrison

Posts

Subscribe

News

  • Access to genomic services
  • GEC-KO on the run
  • 2014 Founders Award for Excellence in Medical Genetics

Events

  • 52nd Ontario College of Family Physicians’ Annual Scientific Assembly
  • 2014 Family Medicine Forum – Nov 13-15 in Quebec City
  • GEC-KO’s November

Recent Posts

  • Family History App in Personalized Medicine (FHAMe): Diabetes
  • Family History App in Personalized Medicine (FHAMe): Cardiovascular disease
  • Genetic Non-Discrimination in Canada

Archives

  • April 2021
  • May 2017
  • October 2016
  • October 2015
  • January 2015
  • November 2014
  • October 2014
  • September 2014
  • August 2014
  • July 2014

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

Tweets

GEC-KO
7 Aug
GEC-KO
@GECKOgenetics

Check out the 🧵 twitter.com/PatientWorthy/…

Expand reply reply retweet retweet favorite favorite
Liz Melchionna, MS, CGC, CG(ASCP)
6 Aug
Liz Melchionna, MS, CGC, CG(ASCP)
@DNAntics

A good chart note w/ patient phenotype details can help turn a VUS into likely pathogenic or likely benign! We love getting that info in the lab; it can help both your patient and those in the future #GeneChat

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
Genomics Education
6 Aug
Genomics Education
@genomicsedu

Visual learners – why not check out our curated playlist of short introductory videos, designed to cover the basics of #genomics. Great for teaching too: orlo.uk/BW7XY pic.twitter.com/Fp64Oo0NAZ

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
Leslie Ordal
6 Aug
Leslie Ordal
@GenCounsNews

dear #GeneChat, currently seeking GCs for low-commitment committee member roles for student capstones! Expertise needed re: GCAs (scope of practice), patient registries, ASL/Deaf patients, and BAP1-TPDS. DM me for more info! pic.twitter.com/tpTcllpFa2

Retweeted by GEC-KORetweeted by GEC-KO
Expand reply reply retweet retweet favorite favorite
Care4Rare Canada
29 Jul
Care4Rare Canada
@C4RCanada

We're excited to announce that our new website is live!🥳 care4rare.ca

Retweeted by GEC-KORetweeted by GEC-KO
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.