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	461.	Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes. [electronic resource] by Annunen, S Körkkö, J Czarny, M Warman, M L Brunner, H G Kääriäinen, H Mulliken, J B Tranebjaerg, L Brooks, D G Cox, G F Cruysberg, J R Curtis, M A Davenport, S L Friedrich, C A Kaitila, I Krawczynski, M R Latos-Bielenska, A Mukai, S Olsen, B R Shinno, N Somer, M Vikkula, M Zlotogora, J Prockop, D J Ala-Kokko, L Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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