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European Journal of Pediatrics|January 2, 1976
Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.European Journal of Pediatrics|August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndromeJ Herrmann, P D Pallister, E F Gilbert, et al.American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.Pageof 57