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- Q90502708 description "article scientifique publié en 2019" @default.
- Q90502708 description "artículu científicu espublizáu n'ochobre de 2019" @default.
- Q90502708 description "im Oktober 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q90502708 description "scientific article published on 02 October 2019" @default.
- Q90502708 description "wetenschappelijk artikel" @default.
- Q90502708 description "наукова стаття, опублікована 2 жовтня 2019" @default.
- Q90502708 description "գիտական հոդված հրատարակված 2019 թվականի հոկտեմբերի 2-ին" @default.
- Q90502708 name "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 name "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 type Item @default.
- Q90502708 label "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 label "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 prefLabel "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 prefLabel "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 P1433 Q90502708-121CCC6B-7246-42CD-8D78-D399322BB6B3 @default.
- Q90502708 P1476 Q90502708-F03D2527-17D9-4BDE-8151-B0B47AE65C9E @default.
- Q90502708 P2093 Q90502708-0171D810-3EEA-4BF9-8E13-AC30EB6CA197 @default.
- Q90502708 P2093 Q90502708-1A85CCF5-C120-4474-9E64-ED074184D17D @default.
- Q90502708 P2093 Q90502708-24AAE0F9-2800-4CDD-8D92-551041DDA232 @default.
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- Q90502708 P2093 Q90502708-52C8EC6E-53FB-4161-AF33-45B8B892D0C2 @default.
- Q90502708 P2093 Q90502708-E14BB64C-B7A6-43A4-A54E-6F6F470AAD72 @default.
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- Q90502708 P304 Q90502708-2E9E447A-43E5-49E0-90F9-7BCF68B37223 @default.
- Q90502708 P31 Q90502708-7854DCBF-2BDC-4E3F-9C32-34E9F2147101 @default.
- Q90502708 P356 Q90502708-C18493FB-94D4-4827-B6F9-EF9014A766B3 @default.
- Q90502708 P433 Q90502708-17E5B009-6C7E-4BC8-A9EB-1D4340D19800 @default.
- Q90502708 P4510 Q90502708-A02E9385-701F-4710-B85D-C9E9C0BACD35 @default.
- Q90502708 P478 Q90502708-A0A2CF5C-865B-4C85-A9C6-7EDD9DD351C8 @default.
- Q90502708 P577 Q90502708-4C2F97CF-E0F5-406A-91BF-668BA11C9117 @default.
- Q90502708 P698 Q90502708-9B1421A2-8D6A-49C6-A7E6-A220D497C04E @default.
- Q90502708 P356 J.EJMG.2019.103782 @default.
- Q90502708 P698 31586465 @default.
- Q90502708 P1433 Q15817083 @default.
- Q90502708 P1476 "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification" @default.
- Q90502708 P2093 "Abdullah Tuli" @default.
- Q90502708 P2093 "Bilgin Yüksel" @default.
- Q90502708 P2093 "Duygu D Boga" @default.
- Q90502708 P2093 "Fatih Gurbuz" @default.
- Q90502708 P2093 "Ihsan Turan" @default.
- Q90502708 P2093 "Leman D Kotan" @default.
- Q90502708 P2093 "Mehmet Tastan" @default.
- Q90502708 P304 "103782" @default.
- Q90502708 P31 Q13442814 @default.
- Q90502708 P356 "10.1016/J.EJMG.2019.103782" @default.
- Q90502708 P433 "4" @default.
- Q90502708 P4510 Q6784807 @default.
- Q90502708 P478 "63" @default.
- Q90502708 P577 "2019-10-02T00:00:00Z" @default.
- Q90502708 P698 "31586465" @default.