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Clinical Genetics|March 1, 1976
Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardationG Neuhäuser, E G Kaveggia, J M Opitz
Pediatric Pathology|January 1, 1985
Omenn disease: termination in lymphomaR Hong, E F Gilbert, J M Opitz
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 Opitz
American Journal of Medical Genetics|March 1, 1982
The neurofaciodigitorenal (NFDR) syndromeN Freire-Maia, M Pinheiro, J M Opitz
European 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 Opitz
American Journal of Medical Genetics|May 1, 1983
Autosomal dominant recurrent encephalopathy of childhoodG Neuhäuser, J M Eichner, J M Opitz
American Journal of Medical Genetics|January 1, 1984
Discovery of a connective tissue dysplasia in the Martin-Bell syndromeJ M Opitz, J M Westphal, A Daniel
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