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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.
Epilepsia|January 1, 1994
Family history of seizures in posttraumatic and alcohol-associated seizure disordersB A Schaumann, J F Annegers, S B Johnson, 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.
American Journal of Medical Genetics|January 1, 1978
An unusual dysplasia-malformation-cancer syndrome in two patientsM V Durkin-Stamm, E F Gilbert, D J Ganick, et al.
Birth Defects Original Article Series|January 1, 1974
Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndromeF T Zugibe, J Herrmann, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1984
Geleophysic dysplasiaJ Spranger, E F Gilbert, S Arya, 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.
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