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