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European 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 OpitzClinical Genetics|March 1, 1976
Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardationG Neuhäuser, E G Kaveggia, J M OpitzZeitschrift Fur Kinderheilkunde|September 11, 1975
Studies of malformation syndromes of man XXXVIII: The BD syndrome. A "new" multiple congenital anomalies/mental retardation syndrome with athetoid cerebral palsyG Neuhäuser, E G Kaveggia, J M OpitzAmerican Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.Zeitschrift Fur Kinderheilkunde|January 1, 1975
Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and reviewR J Hodach, C Viseskul, E F Gilbert, et al.Zeitschrift Fur Kinderheilkunde|September 11, 1975
Generalized gangliosidosis type II (juvenile GM1 gangliosidosis). A pathological, histochemical and ultrastructural studyE F Gilbert, J Varakis, J M Opitz, et al.European Journal of Pediatrics|March 18, 1977
A biologic and genetic study of 40 cases of severe pure mental retardationJ M Becker, E G Kaveggia, E Pendleton, et al.European Journal of Pediatrics|February 21, 1977
Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?G Neuhäuser, G M ZuRhein, E G Kaveggia, et al.Zeitschrift Fur Kinderheilkunde|July 1, 1975
Syndrome of mental retardation, seizures, hypotonic cerebral palsy and megalocorneae, recessively inheritedG Neuhäuser, E G Kaveggia, T D France, et al.Pageof 56