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American Journal of Medical Genetics|April 1, 1989
Polyasplenia complex with mesocardia and renal agenesis in an infant of a diabetic motherA Gonzalez, N Krassikoff, E F Gilbert-BarnessDiseases of the Colon and Rectum|September 1, 1981
Granulomatous appendicitisH M Payan, E F Gilbert, R HafezAmerican Journal of Medical Genetics|June 1, 1987
Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneityK A Aleck, A Grix, C Clericuzio, et al.Human Molecular Genetics|November 1, 1994
A single amino acid substitution (G103D) in the type II collagen triple helix produces Kniest dysplasiaD J Wilkin, R Bogaert, R S Lachman, et al.American Journal of Medical Genetics|November 25, 1992
Spondylometaphyseal dysplasia, Sedaghatian typeJ N Peeden, D L Rimoin, R S Lachman, et al.Pediatric Radiology|November 3, 1998
Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego typeH Kitoh, R S Lachman, S G Brodie, et al.The Journal of Pediatrics|August 1, 1977
Dominant inheritance of cerebral gigantismJ Zonana, J F Sotos, C A Romshe, et al.American Journal of Human Genetics|February 1, 1996
Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasiasJ Hästbacka, A Superti-Furga, W R Wilcox, et al.American Journal of Medical Genetics|March 1, 1986
Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneityD O Sillence, K K Barlow, W G Cole, et al.American Journal of Medical Genetics|March 1, 1988
A new autosomal recessive lethal chondrodystrophy with congenital hydropsC R Greenberg, D L Rimoin, H E Gruber, et al.Pageof 59