Matches in Wikidata for { <http://www.wikidata.org/entity/Q37613086> ?p ?o ?g. }
- Q37613086 description "article científic" @default.
- Q37613086 description "article scientifique" @default.
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- Q37613086 description "artigo científico" @default.
- Q37613086 description "artículu científicu espublizáu en 2013" @default.
- Q37613086 description "bilimsel makale" @default.
- Q37613086 description "scientific article published on March 2013" @default.
- Q37613086 description "vedecký článok" @default.
- Q37613086 description "vetenskaplig artikel" @default.
- Q37613086 description "videnskabelig artikel" @default.
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- Q37613086 description "wissenschaftlicher Artikel" @default.
- Q37613086 description "наукова стаття, опублікована в березні 2013" @default.
- Q37613086 description "научни чланак" @default.
- Q37613086 description "مقالة علمية نشرت في مارس 2013" @default.
- Q37613086 name "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 name "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 name "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
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- Q37613086 label "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 label "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 label "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
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- Q37613086 prefLabel "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 prefLabel "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
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- Q37613086 P356 J.NMD.2013.01.013 @default.
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- Q37613086 P1476 "Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)." @default.
- Q37613086 P2093 "Carsten Bonnemann" @default.
- Q37613086 P2093 "Cornelius F Boerkoel" @default.
- Q37613086 P2093 "Cynthia J Tifft" @default.
- Q37613086 P2093 "David Adams" @default.
- Q37613086 P2093 "Ilda Bajraktari" @default.
- Q37613086 P2093 "John Accardi" @default.
- Q37613086 P2093 "Karin Fuentes Fajardo" @default.
- Q37613086 P2093 "Katy G Meilleur" @default.
- Q37613086 P2093 "Lynne Wolfe" @default.
- Q37613086 P2093 "Mina Jain" @default.
- Q37613086 P2093 "Murat Sincan" @default.
- Q37613086 P2093 "Noor M Tarazi" @default.
- Q37613086 P2093 "Pedro Cruz" @default.
- Q37613086 P2093 "Praveen F Cherukuri" @default.
- Q37613086 P2093 "Sandra Donkervoort" @default.
- Q37613086 P2093 "Tanya J Lehky" @default.
- Q37613086 P2093 "Thomas Markello" @default.
- Q37613086 P2093 "Tyler Mark Pierson" @default.
- Q37613086 P2093 "William A Gahl" @default.
- Q37613086 P2093 "Ying Hu" @default.
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