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European Journal of Pediatrics|November 3, 1976
Studies of malformation syndromes of man XXXXIIB: mother and son affected with the ulnar-mammary syndrome type PallisterC H Gonzalez, J Herrmann, J M OpitzAmerican Journal of Medical Genetics|March 1, 1982
The neurofaciodigitorenal (NFDR) syndromeN Freire-Maia, M Pinheiro, J M OpitzEuropean Journal of Pediatrics|April 26, 1977
Studies of malformation syndromes of man VB: the hypertelorism-hypospadias (BBB) syndrome. Case report and reviewC H Gonzalez, J Herrmann, J M OpitzAmerican Journal of Medical Genetics|May 1, 1983
Autosomal dominant recurrent encephalopathy of childhoodG Neuhäuser, J M Eichner, J M OpitzAmerican Journal of Medical Genetics|January 1, 1984
Discovery of a connective tissue dysplasia in the Martin-Bell syndromeJ M Opitz, J M Westphal, A DanielEuropean Journal of Pediatrics|August 16, 1976
Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis"G Neuhäuser, E G Kaveggia, J M OpitzEuropean Journal of Pediatrics|February 21, 1977
Eye findings in the 13 trisomy syndromeJ C Allen, G Venecia, J M OpitzNeurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.Pediatric Neurology|January 1, 1990
Plasmapheresis with acute inflammatory polyneuropathyB O Khatri, J R Flamini, J K Baruah, et al.Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.Pageof 40