Biomedical subjects
J M Opitz
Publications and source records attributed to J M Opitz.
A partial trisomy 5p syndrome.
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The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
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Study of a child with an "idiopathic" malformation/mental retardation syndrome.
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The Stickler syndrome (hereditary arthroophthalmopathy).
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Letter: Twinning and illegitimacy in C.N.S. defects.
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Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome.
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Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.
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Letter: Parana hard-skin syndrome: study of seven families.
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Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of Zellweger.
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Letter: Immunodeficiency in the cerebro-hepato-renal syndrome of Zellweger.
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Alpha-aminoadipic aciduria, a non-deleterious inborn metabolic defect.
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Generalized lymphangiectosis associated with chylothorax; a possible dysplasia of the lymphatic system.
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A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19).
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Hereditary splenomegaly with hypersplenism.
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Studies of malformation syndromes in man. XXVII. The N syndrome, a "new" multiple congenital anomaly-mental retardation syndrome.
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Cutis marmorata telangiectatica congenita.
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Familial cardiac lipidosis.
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