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American Journal of Medical Genetics. Part A|June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfootW Lu, C A Bacino, B S Richards, et al.American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.The Journal of Pediatrics|October 1, 1978
The phenotypic variability of diastrophic dysplasiaW A Horton, D L Rimoin, R S Lachman, et al.American Journal of Medical Genetics|January 1, 1977
Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVBA I Arbisser, K A Donnelly, C I Scott, et al.American Journal of Human Genetics|November 1, 1981
The Sabinas syndromeR R Howell, A I Arbisser, D S Parsons, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 6, 2000
Cytoskeletal abnormalities in chondrocytes with EXT1 and EXT2 mutationsM A Bernard, D A Hogue, W G Cole, et al.Cell Motility and the Cytoskeleton|February 13, 2001
Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytesM A Bernard, C E Hall, D A Hogue, et al.The Journal of Biological Chemistry|January 10, 1998
The fate of cartilage oligomeric matrix protein is determined by the cell type in the case of a novel mutation in pseudoachondroplasiaB K Maddox, D R Keene, L Y Sakai, et al.Pageof 14