. "v\u011Bdeck\u00FD \u010Dl\u00E1nek"@cs . . . . "articolo scientifico"@it . "Hanan Hamamy" . . "article scientifique"@fr . . "\u043D\u0430\u0443\u043A\u043E\u0432\u0430 \u0441\u0442\u0430\u0442\u0442\u044F, \u043E\u043F\u0443\u0431\u043B\u0456\u043A\u043E\u0432\u0430\u043D\u0430 \u0432 \u043B\u0438\u043F\u043D\u0456 2016"@uk . . . . . . . . "wissenschaftlicher Artikel"@de . "1002309223" . "vedeck\u00FD \u010Dl\u00E1nok"@sk . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree."@nl . . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@ast . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@en . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree."@nl . . . . . . . "article cient\u00EDfic"@ca . . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@ast . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@en . . "\u043D\u0430\u0443\u0447\u043D\u0438 \u0447\u043B\u0430\u043D\u0430\u043A"@sr . . . . . . "art\u00EDculu cient\u00EDficu espubliz\u00E1u en 2016"@ast . . . . . . . . . . . . . . . . . . . . . . . "artigo cient\u00EDfico"@pt . "Stylianos E Antonarakis" . . . . . . . . . . . . . . . . "2016-07-16T00:00:00Z"^^ . . . . "10" . . . "27421267" . . . . . . . . . . . . . . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@en . . . . . . . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree."@nl . . "1" . . . . . . "bilimsel makale"@tr . "\u0645\u0642\u0627\u0644\u0629 \u0639\u0644\u0645\u064A\u0629 \u0646\u0634\u0631\u062A \u0641\u064A 16 \u064A\u0648\u0644\u064A\u0648 2016"@ar . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@en . "scientific article published on 16 July 2016"@en . "vetenskaplig artikel"@sv . . "10.1186/S40246-016-0082-2" . . . . . . . "26" . . "wetenschappelijk artikel"@nl . "videnskabelig artikel"@da . . . . . . . . . . . . "Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree"@ast . . "4947303" . . . . . . . . . . . . . . . "Michel Guipponi" . .