• "Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome
• Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis
• Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders
• Further delineation of the C (trigonocephaly) syndrome
• Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome
• Nager "syndrome" versus "anomaly" and its nosology with the postaxial acrofacial dysostosis syndrome of Genée and Wiedemann
• Polytopic anomalies with agenesis of the lower vertebral column
• Problems of orthodontic care in a patient with Wiedemann-Beckwith-syndrome
• Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases
• The Genée-Wiedemann syndrome, an acrofacial dysostosis--further observation
• The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. 1984
• The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign