1987

ZORA Publication List

Publications

• Hammer, J., Mächler, M., & Schmid, W. (1987). DNA diagnosis of Huntington’s chorea. Application and genetic counseling in 4 involved families. Schweizerische Medizinische Wochenschrift, 117, 2074–2080.
• Schmid, W. (1987). DNA-Diagnostik Schweizerische Medizinische Wochenschrift, 117, 2055–2060.
• Schinzel, A. (1987). Ulnar-mammary syndrome Journal of Medical Genetics, 24, 778–781. https://doi.org/10.1136/jmg.24.12.778
• Hammer, J., Mächler, M., Schmid, W., & Schomig-Spingler, M. (1987). Linked DNA markers in clinical diagnosis of juvenile Huntington’s disease. The Lancet, 330, 1088–1089. https://doi.org/10.1016/s0140-6736(87)91515-7
• Schinzel, A., Illig, R., & Prader, A. (1987). The ulnar‐mammary syndrome: an autosomal dominant pleiotropic gene Clinical Genetics, 32, 160–168. https://doi.org/10.1111/j.1399-0004.1987.tb03347.x
• Schmidtke, J., Krawczak, M., Schwartz, M., Alkan, M., Bonduelle, M., Bühler, E., Chemke, M., Darnedde, T., Domagk, J., Engel, W., Frey, D., Fryburg, K., Halley, D., Hundrieser, J., Ladanyi, L., Libaers, I., Lissens, W., Mächler, M., Malik, N. J., … Voss, R. (1987). Linkage relationships and allelic associations of the cystic fibrosis locus and four marker loci Human Genetics, 76, 337–343. https://doi.org/10.1007/bf00272441
• Schinzel, A., & Opitz, J. M. (1987). Herwigh Rieger, 2 May 1898-1 February 1986 American Journal of Medical Genetics, 27, 749–752. https://doi.org/10.1002/ajmg.1320270402
• Salvoldelli, G., & Schmid, W. (1987). Transabdominale Chorionbiopsie: Erfahrung mit den ersten 200, in der Praxis durchgeführten Biopsien Archives of Gynecology and Obstetrics, 241, S91–S92. https://doi.org/10.1007/bf00930994
• Ritscher, D., Schinzel, A., Boltshauser, E., Briner, J., Arbenz, U., & Sigg, P. (1987). Dandy-Walker (like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: A new syndrome? American Journal of Medical Genetics, 26, 481–491. https://doi.org/10.1002/ajmg.1320260227
• Kläusler, M., Schinzel, A., Gnoinski, W., Hotz, M., & Perko, M. (1987). Dominant vererbte Unterlippenfisteln und Gesichtsspalten (Van-der-Woude-Syn drom). Eine Studie an 52 Fällen Schweizerische Medizinische Wochenschrift, 117, 127–134.
• Schwyzer, U., Binkert, F., Caflisch, U., Baumgartner, B., & Schinzel, A. (1987). Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome Helvetica Paediatrica Acta, 42, 309–315.