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Archives of Pathology & Laboratory Medicine|May 1, 1981
Culture of human glomeruli from patients with metabolic or genetic diseasesT D Oberley, E F Gilbert, C Viseskul, et al.Archives of Pathology & Laboratory Medicine|September 1, 1986
Immunohistochemical studies of rhabdomyosarcomaR Scupham, E F Gilbert, J Wilde, et al.American Journal of Medical Genetics|October 1, 1993
Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosisJ M Opitz, F Mollica, G Sorge, et al.American Journal of Medical Genetics|May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliographyJ M Opitz, A Richieri-da Costa, J M Aase, et al.Clinical Dysmorphology|January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in picturesA Battaglia, J C Carey, D H Viskochil, et al.American Journal of Medical Genetics|January 20, 1997
Autosomal dominant and sporadic radio-ulnar synostosisR Rizzo, V Pavone, G Corsello, et al.European Journal of Pediatrics|September 1, 1976
Analysis of etiologic factors in cerebral palsy with severe mental retardation. I. Analysis of gestational, parturitional and neonatal dataM V Durkin, E G Kaveggia, E Pendleton, et al.Medical and Pediatric Oncology|January 1, 1982
Hodgkin's disease and non-Hodgkin's lymphoma in children and young adults: a clinicopathologic study of 127 casesC Padmalatha, D J Ganick, G R Hafez, et al.Teratology|August 1, 1978
Aortic aneurysm associated with cardiac defects in theophyline stimulated chick embryosS Ishikawa, E F Gilbert, H J Bruyere, et al.Archives of Pathology & Laboratory Medicine|April 1, 1981
Islet cell adenomatosis: a report of two cases and review of the literatureR V Lloyd, V Caceres, T F Warner, et al.Pageof 57