{"id":780,"date":"2016-01-11T14:40:24","date_gmt":"2016-01-11T14:40:24","guid":{"rendered":"https:\/\/www.primarycaregenetics.org\/?page_id=780"},"modified":"2019-06-28T06:23:20","modified_gmt":"2019-06-28T06:23:20","slug":"margmidlun","status":"publish","type":"page","link":"https:\/\/www.primarycaregenetics.org\/?page_id=780&lang=is","title":{"rendered":"Vefkennsla"},"content":{"rendered":"

Mendelskar erf\u00f0ir<\/a><\/p>\n

V\u00edsa\u00f0 \u00ed erf\u00f0aheilbrig\u00f0is\u00fej\u00f3nustu<\/strong><\/p>\n

https:\/\/attendee.gotowebinar.com\/recording\/2084785479224465409<\/a><\/p>\n

A\u00f0 skilja ni\u00f0urst\u00f6\u00f0ur erf\u00f0aranns\u00f3kna<\/strong><\/p>\n

https:\/\/attendee.gotowebinar.com\/recording\/3002563228091384067<\/a><\/p>\n

F\u00f3sturgreining<\/strong><\/p>\n

https:\/\/attendee.gotowebinar.com\/recording\/8377960127566928643<\/a><\/p>\n

 <\/p>\n

Uppt\u00f6kur (\u00e1 ensku).<\/strong><\/p>\n

Taking an appropriate family history to detect possible genetic conditions<\/a><\/p>\n

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.<\/p>\n

Click on https:\/\/attendee.gotowebinar.com\/recording\/6516909152152036354<\/a><\/p>\n

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Recording the family history in a pedigree<\/a><\/p>\n

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.<\/p>\n

Click on https:\/\/attendee.gotowebinar.com\/recording\/8535390399557447938<\/a><\/p>\n

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Understanding common inheritance patterns<\/a><\/p>\n

The common inheritance patterns are explained, along with the risks to family members if a patient is diagnosed with a genetic condition.<\/p>\n

Click on https:\/\/attendee.gotowebinar.com\/recording\/1581348782657205506<\/a><\/p>\n

\n

Understanding prenatal testing for genetic conditions<\/a><\/p>\n

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.<\/p>\n

New non-invasive tests using cell-free fetal DNA (NIPT) are covered.<\/p>\n

https:\/\/attendee.gotowebinar.com\/recording\/7193180271954971906<\/u><\/a><\/p>\n

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Understanding and explaining genetic test results<\/a><\/p>\n

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.<\/p>\n

Click on https:\/\/attendee.gotowebinar.com\/recording\/5825335023012892932<\/a><\/p>\n

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When and how to refer a patient for genetic services.<\/a><\/p>\n

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.<\/p>\n

Click on https:\/\/attendee.gotowebinar.com\/recording\/6398402682586384897<\/a><\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

Mendelskar erf\u00f0ir V\u00edsa\u00f0 \u00ed erf\u00f0aheilbrig\u00f0is\u00fej\u00f3nustu https:\/\/attendee.gotowebinar.com\/recording\/2084785479224465409 A\u00f0 skilja ni\u00f0urst\u00f6\u00f0ur erf\u00f0aranns\u00f3kna https:\/\/attendee.gotowebinar.com\/recording\/3002563228091384067 F\u00f3sturgreining https:\/\/attendee.gotowebinar.com\/recording\/8377960127566928643   Uppt\u00f6kur (\u00e1 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 […]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":26,"comment_status":"closed","ping_status":"closed","template":"template-fullwidth.php","meta":{"ngg_post_thumbnail":0},"_links":{"self":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/780"}],"collection":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=780"}],"version-history":[{"count":18,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/780\/revisions"}],"predecessor-version":[{"id":2846,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/780\/revisions\/2846"}],"wp:attachment":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=780"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}