| 1 | COL11A2, STL3, OSMED |
| Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome). | |
| Pihlajamaa T, et al. | |
| Am J Med Genet 80 : 115-120. 1998 | |
| 2 | COL11A2, STL3, OSMED |
| Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. | |
| Vikkula M, et al. | |
| Cell 80 : 431-437. 1995 | |
| 3 | COL11A2, STL3 |
| A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene. | |
| Brunner HG, et al. | |
| Hum Mol Genet 3 : 1561-1564. 1994 | |