Matches in Wikidata for { <http://www.wikidata.org/entity/Q37058516> ?p ?o ?g. }
- Q37058516 description "article científic" @default.
- Q37058516 description "article scientifique" @default.
- Q37058516 description "articolo scientifico" @default.
- Q37058516 description "artigo científico" @default.
- Q37058516 description "artículu científicu espublizáu en 2015" @default.
- Q37058516 description "bilimsel makale" @default.
- Q37058516 description "scientific article published on 26 August 2015" @default.
- Q37058516 description "vedecký článok" @default.
- Q37058516 description "vetenskaplig artikel" @default.
- Q37058516 description "videnskabelig artikel" @default.
- Q37058516 description "vědecký článek" @default.
- Q37058516 description "wetenschappelijk artikel" @default.
- Q37058516 description "wissenschaftlicher Artikel" @default.
- Q37058516 description "наукова стаття, опублікована в серпні 2015" @default.
- Q37058516 description "научни чланак" @default.
- Q37058516 description "مقالة علمية نشرت في 26 أغسطس 2015" @default.
- Q37058516 name "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
- Q37058516 name "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
- Q37058516 name "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
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- Q37058516 label "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
- Q37058516 label "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
- Q37058516 label "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
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- Q37058516 prefLabel "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
- Q37058516 prefLabel "The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant." @default.
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