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Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.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.Journal of Child Neurology|May 1, 1996
Severity of medical and neurologic complications as a determinant of neurodevelopmental outcome at 6 and 12 months in very low birth weight infantsA E Anderson, S R Wildin, M Woodside, 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.Pageof 21