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Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.American Journal of Human Genetics|September 16, 1999
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.Pageof 30