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American Journal of Medical Genetics|March 1, 1993
Hearing loss and temporal bone structure in achondroplasiaM Shohat, E Flaum, S R Cobb, et al.
American Journal of Respiratory Cell and Molecular Biology|June 1, 1993
Aspartic proteinases in normal lung and interstitial pulmonary diseasesF Bosi, E Silini, M Luisetti, et al.
Scandinavian Journal of Gastroenterology. Supplement|January 1, 1985
The histology of the stomach in symptomatic patients after gastric surgery: a model to assess selective patterns of gastric mucosal injuryW M Weinstein, K L Buch, J Elashoff, et al.
The Biochemical Journal|September 15, 1988
Identification of the aspartic proteinases from human erythrocyte membranes and gastric mucosa (slow-moving proteinase) as catalytically equivalent to cathepsin ER A Jupp, A D Richards, J Kay, et al.
Gastroenterology|December 1, 1986
Familial visceral neuropathy with autosomal dominant transmissionE A Mayer, M D Schuffler, J I Rotter, et al.
Gastroenterology|October 1, 1989
Geographic origins of Jewish patients with inflammatory bowel diseaseM P Roth, G M Petersen, C McElree, et al.
American 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.
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