Authors: Tremain, N Korkko, J Ibberson, D Kopen, GC DiGirolamo, C Phinney, DG

Citation: N. Tremain et al., MicroSAGE analysis of 2,353 expressed genes in a single cell-derived colony of undifferentiated human mesenchymal stem cells reveals mRNAs of multiple cell lineages, STEM CELLS, 19(5), 2001, pp. 408-418

Authors: Unger, S Korkko, J Krakow, D Lachman, RS Rimoin, DL Cohn, DH

Citation: S. Unger et al., Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita, AM J MED G, 104(2), 2001, pp. 140-146

Authors: Pallos, D Hart, PS Cortelli, JR Vian, S Wright, JT Korkko, J Brunoni, D Hart, TC

Citation: D. Pallos et al., Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfectaand dentinogenesis imperfecta, ARCH ORAL B, 46(5), 2001, pp. 459-470

Authors: Korkko, J Cohn, DH Ala-Kokko, L Krakow, D Prockop, DJ

Citation: J. Korkko et al., Widely distributed mutations in the COL2A1 gene produce achondrogenesis type II/hypochondrogenesis, AM J MED G, 92(2), 2000, pp. 95-100

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