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The New England Journal of Medicine|January 11, 1979
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorderJ I Rotter, J Q Sones, I M Samloff, et al.American Journal of Medical Genetics|January 1, 1980
Congenital macular colobomas and short-limb skeletal dysplasiaR D Smith, R M Fineman, D O Sillence, et al.Journal of Mental Deficiency Research|December 1, 1977
Chemical analysis of an angiofibroma from a patient with tuberous sclerosisM H Fischer, J S Fortune, S H Foster, et al.European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.Journal of Applied Toxicology : JAT|April 1, 1986
The teratogenic effect of phenobarbital on the embryonic chick heartT Nishikawa, H J Bruyere, Y Takagi, et al.American Journal of Medical Genetics|November 1, 1984
Acrofacial dysplasia resembling geleophysic dysplasiaJ Spranger, E F Gilbert, S Flatz, et al.European Journal of Pediatrics|July 1, 1977
Studies of malformation syndromes of man XLVII: disappearance of spermatogonia in the Fanconi anemia syndromeG J Bargman, N T Shahidi, E F Gilbert, et al.Thorax|June 1, 1980
Acquired double-barrel oesophagus in epidermolysis bullosa dystrophicaR B Warren, T F Warner, E F Gilbert, et al.American Heart Journal|September 1, 1991
Tricuspid atresia: association with persistent truncus arteriosusP S Rao, J M Levy, E Nikicicz, et al.Journal of Pediatric Gastroenterology and Nutrition|January 1, 1989
Alpha 1-antitrypsin deficiency and the PiMS phenotype: case report and literature reviewM F Gourley, G R Gourley, E F Gilbert, et al.Pageof 59