{"id":12202,"date":"2021-10-29T15:52:31","date_gmt":"2021-10-29T13:52:31","guid":{"rendered":"https:\/\/www.humangenetik-umg.de\/?p=12202"},"modified":"2021-10-29T15:52:31","modified_gmt":"2021-10-29T13:52:31","slug":"tp63-by-cleft-tongue","status":"publish","type":"post","link":"https:\/\/www.humangenetik-umg.de\/en\/tp63-by-cleft-tongue\/","title":{"rendered":"TP63 variant causes novel phenotype dominated by cleft tongue"},"content":{"rendered":"<div class=\"wpb-content-wrapper\">[vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2021\/10\/visual-tp63-en.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=&#8221;.vc_custom_1635515345579{margin-bottom: 0px !important;}&#8221;]<strong>Familial cleft tongue caused by a unique translation initiation codon variant in TP63<\/strong><br \/>\nSchmidt J, Schreiber G, Altm\u00fcller J, Thiele H, N\u00fcrnberg P, Li Y, Kaulfu\u00df S, Funke R, Wilken B, Yigit G, Wollnik B.<br \/>\n<em>Eur J Hum Genet<\/em>. 2021 Oct 11. doi: 10.1038\/s41431-021-00967-x. Epub ahead of print.<\/p>\n[mk_button dimension=&#8221;flat&#8221; size=&#8221;medium&#8221; icon=&#8221;mk-icon-long-arrow-right&#8221; icon_anim=&#8221;side&#8221; url=&#8221;https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/34629465&#8243; target=&#8221;_blank&#8221; bg_color=&#8221;#006699&#8243; btn_hover_bg=&#8221;#000000&#8243; btn_hover_txt_color=&#8221;#ffffff&#8221;]Article in PubMed[\/mk_button][mk_padding_divider size=&#8221;30&#8243;][\/vc_column_text][\/vc_column][\/vc_row]\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][mk_image src=&#8221;https:\/\/www.humangenetik-umg.de\/wp-content\/uploads\/2021\/10\/visual-tp63-en.png&#8221; image_size=&#8221;full&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][mk_padding_divider size=&#8221;30&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=&#8221;.vc_custom_1635515345579{margin-bottom: 0px !important;}&#8221;]Familial cleft tongue caused by a unique translation initiation codon variant in TP63 Schmidt J, Schreiber G, Altm\u00fcller J, Thiele H, N\u00fcrnberg P, Li Y, Kaulfu\u00df S, Funke R, Wilken B, Yigit G, Wollnik B. Eur J Hum Genet. 2021 Oct 11. doi: 10.1038\/s41431-021-00967-x. Epub ahead of print. [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[51],"tags":[],"class_list":["post-12202","post","type-post","status-publish","format-standard","hentry","category-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>TP63 variant causes novel phenotype dominated by cleft tongue - Institut f\u00fcr Humangenetik<\/title>\n<meta name=\"description\" content=\"Study identifies TP63 variant causing a novel phenotype dominated by cleft tongue\" \/>\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.humangenetik-umg.de\/en\/tp63-by-cleft-tongue\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"TP63 variant causes novel phenotype dominated by cleft tongue - 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