Matches in Wikidata for { <http://www.wikidata.org/entity/Q74127603> ?p ?o ?g. }
Showing items 1 to 77 of
77
with 100 items per page.
- Q74127603 description "articolo scientifico (pubblicato il 1998)" @default.
- Q74127603 description "artikull shkencor i botuar më 01 janar 1998" @default.
- Q74127603 description "artículu científicu espublizáu en xineru de 1998" @default.
- Q74127603 description "im Jahr 1998 veröffentlichter wissenschaftlicher Artikel" @default.
- Q74127603 description "scientific article published on 01 January 1998" @default.
- Q74127603 description "wetenschappelijk artikel" @default.
- Q74127603 description "наукова стаття, опублікована в січні 1998" @default.
- Q74127603 name "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 name "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 name "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 type Item @default.
- Q74127603 label "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 label "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 label "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 prefLabel "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 prefLabel "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 prefLabel "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 P1433 Q74127603-72D787B6-098A-4190-9C22-25E331D281CD @default.
- Q74127603 P1476 Q74127603-9AC40DD0-A7EA-4A37-91C2-DA5863BBC25C @default.
- Q74127603 P2093 Q74127603-26FB689D-FC52-44FF-BCCE-7ECCFC91523E @default.
- Q74127603 P2093 Q74127603-30054CC5-8860-4FB4-A1E5-B43B02B7A990 @default.
- Q74127603 P2093 Q74127603-5A2D108D-72EE-4521-BB39-361D01E240BA @default.
- Q74127603 P2093 Q74127603-E735384E-3C41-4C37-A3CD-48250D9C34A5 @default.
- Q74127603 P2860 Q74127603-1D65C374-EC08-4AB9-9D26-95FE1976AF11 @default.
- Q74127603 P2860 Q74127603-20ADB4EC-A36A-4A3B-8C98-1D536E1ADE8B @default.
- Q74127603 P2860 Q74127603-22FF3C2E-6A25-4FD5-8E95-4F74040694C6 @default.
- Q74127603 P2860 Q74127603-30FFCA77-CEF1-4FF3-BBDB-85140E9BC830 @default.
- Q74127603 P2860 Q74127603-3B7CC4D0-9628-4942-A3FE-837169117E8F @default.
- Q74127603 P2860 Q74127603-4561C2C1-94F8-4AF8-B851-8B43767B4C47 @default.
- Q74127603 P2860 Q74127603-530213DD-CBF9-4F7B-8533-D6D0AB2F5565 @default.
- Q74127603 P2860 Q74127603-64C06CC9-3708-4AB9-BB16-9E3233FD364D @default.
- Q74127603 P2860 Q74127603-7A8D1FFF-7D4D-45BC-9B95-F55FC1189693 @default.
- Q74127603 P2860 Q74127603-8E3C07D3-810A-443E-A472-29CD4DE158AC @default.
- Q74127603 P2860 Q74127603-8F0EB54D-5FB8-4F6A-BE9D-2CE4514A15FA @default.
- Q74127603 P2860 Q74127603-B5021064-AC7C-4F5A-BD59-C023C3547FDC @default.
- Q74127603 P2860 Q74127603-B6F07B46-C52F-4C3E-8DBA-D3130CC98558 @default.
- Q74127603 P2860 Q74127603-B880BCF0-DC9D-486A-83B9-D813317664F1 @default.
- Q74127603 P2860 Q74127603-E3FE1C0F-2825-494A-8E9C-780CD263405C @default.
- Q74127603 P2860 Q74127603-FB04441C-3FB6-491D-A252-D81251AFF57D @default.
- Q74127603 P304 Q74127603-E24C3A3B-64B8-44CF-8E9B-5DBBD640D5E4 @default.
- Q74127603 P31 Q74127603-BC386B1F-CAE3-4082-A67C-5E9EEF809C11 @default.
- Q74127603 P356 Q74127603-AE146882-1272-45D2-AC8F-C242FF27E71D @default.
- Q74127603 P478 Q74127603-6118386A-826D-4167-9BDA-C03BEC95FFFA @default.
- Q74127603 P50 Q74127603-120CF26D-C008-403F-94D4-0D80C253BDAE @default.
- Q74127603 P577 Q74127603-E2BD08BF-E245-4702-B5F3-52260808D17A @default.
- Q74127603 P698 Q74127603-16CD0712-FA1D-4FFB-8859-368AE1772ED6 @default.
- Q74127603 P356 HUMU.1380110112 @default.
- Q74127603 P698 9452033 @default.
- Q74127603 P1433 Q5937269 @default.
- Q74127603 P1476 "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
- Q74127603 P2093 "K Kainulainen" @default.
- Q74127603 P2093 "L Karttunen" @default.
- Q74127603 P2093 "L Peltonen" @default.
- Q74127603 P2093 "T Ukkonen" @default.
- Q74127603 P2860 Q22066207 @default.
- Q74127603 P2860 Q26778460 @default.
- Q74127603 P2860 Q33905897 @default.
- Q74127603 P2860 Q34337855 @default.
- Q74127603 P2860 Q36713104 @default.
- Q74127603 P2860 Q36768408 @default.
- Q74127603 P2860 Q37084846 @default.
- Q74127603 P2860 Q38297126 @default.
- Q74127603 P2860 Q38317023 @default.
- Q74127603 P2860 Q39514050 @default.
- Q74127603 P2860 Q40518319 @default.
- Q74127603 P2860 Q40647569 @default.
- Q74127603 P2860 Q40934983 @default.
- Q74127603 P2860 Q69393557 @default.
- Q74127603 P2860 Q70554031 @default.
- Q74127603 P2860 Q71354907 @default.
- Q74127603 P304 "S34-7" @default.
- Q74127603 P31 Q13442814 @default.
- Q74127603 P356 "10.1002/HUMU.1380110112" @default.
- Q74127603 P478 "Suppl 1" @default.
- Q74127603 P50 Q4981688 @default.
- Q74127603 P577 "1998-01-01T00:00:00Z" @default.
- Q74127603 P698 "9452033" @default.