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dc.contributor.authorWiseman, K.
dc.contributor.authorUstek, D.
dc.contributor.authorThomas, N. S. T.
dc.contributor.authorSpurlock, G.
dc.contributor.authorMacDonald, M.
dc.contributor.authorUpadhyaya, Meena
dc.date.accessioned2021-03-04T09:29:56Z
dc.date.available2021-03-04T09:29:56Z
dc.identifier.citationUpadhyaya M., Thomas N. S. T. , Wiseman K., Spurlock G., MacDonald M., Ustek D., "A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere", British Human Genetics Conference, York, Sierra Leone, 18 - 20 Eylül 2006, cilt.43
dc.identifier.othervv_1032021
dc.identifier.otherav_6890fef7-1d07-445d-b33b-910e8f4a4e62
dc.identifier.urihttp://hdl.handle.net/20.500.12627/72465
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.titleA large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume43
dc.contributor.firstauthorID132753


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