{"id":6306,"date":"2016-08-05T09:45:55","date_gmt":"2016-08-05T07:45:55","guid":{"rendered":"http:\/\/igcz.poznan.pl\/en\/?p=6306"},"modified":"2016-08-05T10:01:52","modified_gmt":"2016-08-05T08:01:52","slug":"6306","status":"publish","type":"post","link":"https:\/\/igcz.poznan.pl\/en\/new-publication\/6306\/","title":{"rendered":"<strong>New publication:<\/strong> Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency"},"content":{"rendered":"<p>Ziemnicka K, Budny B, Drobnik K, Baszko-B\u0142aszyk D, Stajgis M, Katulska K, Wa\u015bko R, Wrotkowska E, <strong>S\u0142omski R<\/strong>, Rucha\u0142a M<br \/>\n<span style=\"font-size: 10pt; color: #808080;\">J. Appl. Genet., 2016 AUg;57(3):373-81, Epub 2015 Nov 25; IF <strong>1.929<\/strong>; MNiSW <strong>20<\/strong><\/span><!--more--><\/p>\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26608600\">Link to publication<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ziemnicka K, Budny B, Drobnik K, Baszko-B\u0142aszyk D, Stajgis M, Katulska K, Wa\u015bko R, Wrotkowska E, S\u0142omski R, Rucha\u0142a M J. Appl. Genet., 2016 AUg;57(3):373-81, Epub 2015 Nov 25; IF 1.929; MNiSW 20<\/p>\n","protected":false},"author":103,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[135],"tags":[],"class_list":["post-6306","post","type-post","status-publish","format-standard","hentry","category-new-publication"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>New publication: Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency - Institute of Human Genetics Polish Academy of Sciences<\/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:\/\/igcz.poznan.pl\/en\/new-publication\/6306\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"New publication: Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency - Institute of Human Genetics Polish Academy of Sciences\" \/>\n<meta property=\"og:description\" content=\"Ziemnicka K, Budny B, Drobnik K, Baszko-B\u0142aszyk D, Stajgis M, Katulska K, Wa\u015bko R, Wrotkowska E, S\u0142omski R, Rucha\u0142a M J. 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