{"id":1425805,"date":"2022-01-04T08:48:14","date_gmt":"2022-01-04T07:48:14","guid":{"rendered":"https:\/\/staging-wp-int.laboklin.com\/products\/genetics\/genetic-combinations\/dog\/combination-labradoodle\/"},"modified":"2022-01-04T08:48:14","modified_gmt":"2022-01-04T07:48:14","slug":"combination-labradoodle","status":"publish","type":"page","link":"https:\/\/laboklin.com\/fr\/prestations\/genetique\/combinaison-genetique\/dog\/combination-labradoodle\/","title":{"rendered":"Combination Labradoodle"},"content":{"rendered":"<h3 class=\"csc-firstHeader\">Combination Labradoodle<\/h3><p><span>LABOKLIN Service ID: 8743<\/span><\/p><p class=\"bodytext\">The following tests are included in this combination:<br \/>\r\n<br \/>\r\nCentronuclear myopathy (CNM), Degenerative myelopathy (exon 2), Exercise induced collapse (EIC), Hereditary nasal parakeratosis (HNPK), Neonatal encephalopathy with seizures (NEWS), Skeletal dysplasia 2 (SD2), von Willebrand disease type I (vWD 1), Progressive retinal atrophy (prcd-PRA) and Progressive retinal atrophy (rcd4-PRA)<\/p><table class=\"tx-laboklinleistung-table contenttable contenttable-2\" style=\"margin-top: 35px;\"><tr><td class=\"td-0\"><strong>Breed list<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">Labradoodle<\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Heredity<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">Further information could be found in the description of the corresponding genetic test. <\/p><\/td><\/tr><tr><td class=\"td-0\"><strong>Duration<\/strong><\/td><td class=\"td-1\"><p class=\"bodytext\">1 - 2 weeks after arrival of the sample in the lab<\/p><\/td><\/tr><\/table>\n","protected":false},"excerpt":{"rendered":"<p>Combination LabradoodleLABOKLIN Service ID: 8743The following tests are included in this combination: Centronuclear myopathy (CNM), Degenerative myelopathy (exon 2), Exercise induced collapse (EIC), Hereditary nasal parakeratosis (HNPK), Neonatal encephalopathy with seizures (NEWS), Skeletal dysplasia 2 (SD2), von Willebrand disease type I (vWD 1), Progressive retinal atrophy (prcd-PRA) and Progressive retinal atrophy (rcd4-PRA)Breed listLabradoodleHeredityFurther information could&hellip;<\/p>\n","protected":false},"author":10,"featured_media":0,"parent":1418890,"menu_order":6,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","footnotes":""},"class_list":["post-1425805","page","type-page","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1425805","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/users\/10"}],"replies":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/comments?post=1425805"}],"version-history":[{"count":0,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1425805\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/pages\/1418890"}],"wp:attachment":[{"href":"https:\/\/laboklin.com\/fr\/wp-json\/wp\/v2\/media?parent=1425805"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}