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Upptökur (á ensku).
Taking an appropriate family history to detect possible genetic conditions
In this webinar, we discuss how to take a family history, effectively and systematically, to ensure you can identify patients at increased risk of a genetic condition.
Click on https://attendee.gotowebinar.com/recording/6516909152152036354
Recording the family history in a pedigree
In this webinar, we discuss how to record the family history, effectively and systematically, using accepted pedigree symbols. You will have the chance to practice yourself.
Click on https://attendee.gotowebinar.com/recording/8535390399557447938
Understanding common inheritance patterns
The common inheritance patterns are explained, along with the risks to family members if a patient is diagnosed with a genetic condition.
Click on https://attendee.gotowebinar.com/recording/1581348782657205506
Understanding prenatal testing for genetic conditions
In this webinar, we discuss the various types of prenatal tests, including population screening and specific tests to identify a fetus at high risk of a genetic condition known to be in the family.
New non-invasive tests using cell-free fetal DNA (NIPT) are covered.
Understanding and explaining genetic test results
In this webinar, we discuss the types of genetic tests that might be offered to your patient and the possible results, to help you explain those.
Click on https://attendee.gotowebinar.com/recording/5825335023012892932
When and how to refer a patient for genetic services.
Would you know who to refer to genetic services, or how to find those services? In this webinar we discuss types of patients who benefit from referral and how you can identify where to refer.
Click on https://attendee.gotowebinar.com/recording/6398402682586384897