1983

ZORA Publication List

Publications

• Schinzel, Albert (1983). Catalogue of Unbalanced Chromosome Aberrations in Man. New York: De Gruyter.
• Schmid, Werner; Widmer, O (1983). School and occupational history of 30 patients with Klinefelter's syndrome. Significance of early diagnosis. Schweizerische Medizinische Wochenschrift, 113(48):1790-1794.
• Schmid, Werner; Tenconi, Romano; Baccichetti, Carlo; Caufin, Daniele; Schinzel, Albert (1983). Ring chromosome 21 in phenotypically apparently normal persons: Report of two families from Switzerland and Italy. American Journal of Medical Genetics, 16(3):323-329.
• Fraccaro, Marco; Zuffardi, Orsetta; Bühler, E; Schinzel, Albert; Simoni, G; Witkowski, R; Bonifaci, E; Caufin, Daniele; Cignacco, G; Delendi, N; Gargantini, L; Losanowa, T; Marca, L; Ullrich, E; Vigi, V (1983). Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment. Human Genetics, 64(4):388-394.
• Hall, J G; Reed, S D; McGillivray, B C; Herrmann, J; Partington, M W; Schinzel, Albert; Shapiro, J; Weaver, D D; Opitz, John M (1983). Part II. Amyoplasia: Twinning in amyoplasia—a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins. American Journal of Medical Genetics, 15(4):591-599.
• Hall, J G; Reed, S D; McGillivray, B C; Herrmann, J; Partington, M W; Schinzel, Albert; Shapiro, J; Weaver, D D; Opitz, John M (1983). Part II. Amyoplasia: Twinning in amyoplasia—a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins. American Journal of Medical Genetics, 15(4):591-599.
• Schoenle, E; Schmid, Werner; Schinzel, Albert; Mahler, Michael; Ritter, M; Schenker, T; Metaxas, M; Froesch, P; Froesch, E R (1983). 46,XX/46,XY chimerism in a phenotypically normal man. Human Genetics, 64(1):86-89.
• Houston, C Stuart; Opitz, John M; Spranger, Jürgen W; Macpherson, Roderick I; Reed, Martin H; Gilbert, Enid F; Herrmann, Jürgen; Schinzel, Albert (1983). The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971. American Journal of Medical Genetics, 15(1):3-28.
• Schmid, Werner; Bächler, A; Frey, D; Gerth, Hans Jörg; Prim, J; Hänseler, A; Augsburger, T (1983). Genetische, medizinische und psychosoziale Faktoren bei der Lernbehinderung eines Jahrgangs von Elfjährigen (Winterthurer Studie). Acta paedopsychiatrica, 49(1-2):9-45.
• Schinzel, Albert (1983). Difetti strutturali nei gemelli. Prospettive in pediatria, 50:89-94.
• Zollinger, A; Schmid, Werner; Vilan, J; Sorger, Bettina; Knoblauch, M (1983). X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism. Schweizerische Medizinische Wochenschrift, 113(7):238-44.
• Schinzel, Albert; Savoldelli, Guido; Briner, Jakob; Sigg, Peter; Massini, Carlo; Opitz, John M (1983). Antley‐Bixler syndrome in sisters: A term newborn and a prenatally diagnosed fetus. American Journal of Medical Genetics, 14(1):139-147.
• Schmid, Werner (1983). Schulstress: allgemeine Gesichtspunkte und ein Blick in das Material der "Winterthurer Studie". Bildungsforschung und Bildungspraxis, 5(2):147-156.
• Schinzel, Albert A (1983). Cardiovascular defects associated with chromosomal aberrations and malformation syndromes. Progress in Medical Genetics, 5:303-379.