1983

ZORA Publikationsliste

Publikationen

• Schinzel, A. (1983). Catalogue of Unbalanced Chromosome Aberrations in Man De Gruyter. https://doi.org/10.1515/9783112329047
• Schmid, W., & Widmer, O. (1983). School and occupational history of 30 patients with Klinefelter’s syndrome. Significance of early diagnosis. Schweizerische Medizinische Wochenschrift, 113, 1790–1794.
• Schmid, W., Tenconi, R., Baccichetti, C., Caufin, D., & Schinzel, A. (1983). Ring chromosome 21 in phenotypically apparently normal persons: Report of two families from Switzerland and Italy American Journal of Medical Genetics, 16, 323–329. https://doi.org/10.1002/ajmg.1320160305
• Fraccaro, M., Zuffardi, O., Bühler, E., Schinzel, A., Simoni, G., Witkowski, R., Bonifaci, E., Caufin, D., 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, 388–394. https://doi.org/10.1007/bf00292373
• Hall, J. G., Reed, S. D., McGillivray, B. C., Herrmann, J., Partington, M. W., Schinzel, A., Shapiro, J., Weaver, D. D., & Opitz, J. 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, 591–599. https://doi.org/10.1002/ajmg.1320150408
• Hall, J. G., Reed, S. D., McGillivray, B. C., Herrmann, J., Partington, M. W., Schinzel, A., Shapiro, J., Weaver, D. D., & Opitz, J. 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, 591–599. https://doi.org/10.1002/ajmg.1320150408
• Schoenle, E., Schmid, W., Schinzel, A., Mahler, M., 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, 86–89. https://doi.org/10.1007/bf00289485
• Houston, C. S., Opitz, J. M., Spranger, J. W., Macpherson, R. I., Reed, M. H., Gilbert, E. F., Herrmann, J., & Schinzel, A. (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, 3–28. https://doi.org/10.1002/ajmg.1320150103
• Schmid, W., Bächler, A., Frey, D., Gerth, H. J., Prim, J., Hänseler, A., & Augsburger, T. (1983). Genetische, medizinische und psychosoziale Faktoren bei der Lernbehinderung eines Jahrgangs von Elfjährigen (Winterthurer Studie) Acta paedopsychiatrica, 49, 9–45.
• Schinzel, A. (1983). Difetti strutturali nei gemelli Prospettive in pediatria, 50, 89–94.
• Zollinger, A., Schmid, W., Vilan, J., Sorger, B., & Knoblauch, M. (1983). X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism Schweizerische Medizinische Wochenschrift, 113, 238–244.
• Schulstress: allgemeine Gesichtspunkte und ein Blick in das Material der “Winterthurer Studie.” Bildungsforschung und Bildungspraxis, 5, 147–156.
• Schinzel, A., Savoldelli, G., Briner, J., Sigg, P., Massini, C., & Opitz, J. M. (1983). Antley‐Bixler syndrome in sisters: A term newborn and a prenatally diagnosed fetus American Journal of Medical Genetics, 14, 139–147. https://doi.org/10.1002/ajmg.1320140119
• Schinzel, A. A. (1983). Cardiovascular defects associated with chromosomal aberrations and malformation syndromes Progress in Medical Genetics, 5, 303–379.