{"id":15923,"date":"2024-01-30T12:38:24","date_gmt":"2024-01-30T11:38:24","guid":{"rendered":"https:\/\/www.cutislaxa.org\/?p=15923"},"modified":"2024-02-19T13:16:48","modified_gmt":"2024-02-19T12:16:48","slug":"entrevista-de-dave-jacob-sobre-el-podcast-grey-genetics-historias-de-pacientes","status":"publish","type":"post","link":"https:\/\/www.cutislaxa.org\/es\/entrevista-de-dave-jacob-sobre-el-podcast-grey-genetics-historias-de-pacientes\/","title":{"rendered":"Entrevista de Dave Jacob sobre el podcast Grey Genetics Historias de Pacientes"},"content":{"rendered":"<p style=\"text-align: center;\">Dave Jacob, fundador de ThinkGenetic, apareci\u00f3 en el Grey Genetics Patient Stories Podcast el 30 de enero de 2024.<\/p>\n<p style=\"text-align: center;\">\u00c9l relata su viaje diagn\u00f3stico, que finalmente llev\u00f3 a un diagn\u00f3stico de Cutis Laxa.<\/p>\n<p style=\"text-align: center;\">Comparte c\u00f3mo su experiencia personal como paciente de enfermedades raras inspir\u00f3<\/p>\n<p style=\"text-align: center;\">el inicio de ThinkGenetic Inc. y ThinkGenetic Foundation.<\/p>\n<p style=\"text-align: center;\">Escuchar (en ingl\u00e9s)<\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/www.greygenetics.com\/a-late-diagnosis-of-cutis-laxa-and-the-creation-of-thinkgenetics\/\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-15902 aligncenter\" src=\"https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-300x300.jpg\" alt=\"\" width=\"300\" height=\"300\" srcset=\"https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-300x300.jpg 300w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-80x80.jpg 80w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-768x771.jpg 768w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-36x36.jpg 36w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-180x180.jpg 180w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob-702x705.jpg 702w, https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2024\/02\/Interview-Dave-Jacob.jpg 786w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Dave Jacob, fundador de ThinkGenetic, apareci\u00f3 en el Grey Genetics Patient Stories Podcast el 30 de enero de 2024. \u00c9l relata su viaje diagn\u00f3stico, que finalmente llev\u00f3 a un diagn\u00f3stico de Cutis Laxa. Comparte c\u00f3mo su experiencia personal como paciente de enfermedades raras inspir\u00f3 el inicio de ThinkGenetic Inc. y ThinkGenetic Foundation. Escuchar (en ingl\u00e9s)<\/p>\n","protected":false},"author":2,"featured_media":12386,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[81,76,103],"tags":[],"class_list":["post-15923","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medios-de-comunicacion","category-noticias","category-video-es"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Entrevista de Dave Jacob sobre el podcast Grey Genetics Historias de Pacientes - CUTIS LAXA INTERNATIONALE<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.cutislaxa.org\/fr\/?p=15920\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Entrevista de Dave Jacob sobre el podcast Grey Genetics Historias de Pacientes - CUTIS LAXA INTERNATIONALE\" \/>\n<meta property=\"og:description\" content=\"Dave Jacob, fundador de ThinkGenetic, apareci\u00f3 en el Grey Genetics Patient Stories Podcast el 30 de enero de 2024. \u00c9l relata su viaje diagn\u00f3stico, que finalmente llev\u00f3 a un diagn\u00f3stico de Cutis Laxa. Comparte c\u00f3mo su experiencia personal como paciente de enfermedades raras inspir\u00f3 el inicio de ThinkGenetic Inc. y ThinkGenetic Foundation. 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