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Results: 3

Authors: Czarny-Ratajczak, M Lohiniva, J Rogala, P Kozlowski, K Perala, M Carter, L Spector, TD Kolodziej, L Seppanen, U Glazar, R Krolewski, J Latos-Bielenska, A Ala-Kokko, L
Citation: M. Czarny-ratajczak et al., A mutation in COL9A1 causes multiple epiphyseal dysplasia: Further evidence for locus heterogeneity, AM J HU GEN, 69(5), 2001, pp. 969-980

Authors: Kusz, K Kotecki, M Wojda, A Szarras-Czapnik, M Latos-Bielenska, A Warenik-Szymankiewicz, A Ruszczynska-Wolska, A Jaruzelska, J
Citation: K. Kusz et al., Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome, J MED GENET, 36(6), 1999, pp. 452-456

Authors: Annunen, S Korkko, J Czarny, M Warman, ML Brunner, HG Kaariainen, H Mulliken, JB Tranebjaerg, L Brooks, DG Cox, GF Cruysberg, JR Curtis, MA Davenport, SLH Friedrich, CA Kaitila, I Krawczynski, MR Latos-Bielenska, A Mukai, S Olsen, BR Shinno, N Somer, M Vikkula, M Zlotogora, J Prockop, DJ Ala-Kokko, L
Citation: S. Annunen et al., Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes, AM J HU GEN, 65(4), 1999, pp. 974-983
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