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The American Journal of Surgical Pathology|April 1, 1987
Giant cell fibroblastoma. A distinctive, recurrent tumor of childhoodR B Dymock, P W Allen, J W Stirling, et al.American Journal of Medical Genetics|January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literatureP Steinbach, W N Adkins, H Caspar, et al.Pediatric Radiology|January 1, 1985
Narrow trachea in mucopolysaccharidosesM E Peters, S Arya, L O Langer, et al.Teratology|August 1, 1983
Cardiovascular malformations associated with administration of prenalterol to young chick embryosH J Bruyere, R Matsuoka, E Carlsson, et al.American Journal of Clinical Pathology|July 1, 1991
Comparison of an isoelectric focusing technique and high-performance liquid chromatography for determination of fetal hemoglobin levelsE F Gilbert-Barness, K S Kenison, E Shrago, et al.American Journal of Diseases of Children (1960)|March 1, 1986
Familial lung disease associated with proliferation and desquamation of type II pneumonocytesP M Farrell, E F Gilbert, J J Zimmerman, et al.American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.Human Pathology|April 1, 1987
Thyrocalcitonin-containing cells in the Di George anomalyB A Burke, D Johnson, E F Gilbert, et al.Pageof 57