1980

ZORA Publication List

Publications

• Schinzel, A. (1980). Complete and partial trisomy 8 Clinical Genetics, 18, 314. https://doi.org/10.1111/j.1399-0004.1980.tb00891.x
• Passarge, E., & Vogel, F. (1980). The delivery of genetic counseling services in Europe Human Genetics, 56, 1–5. https://doi.org/10.1007/bf00281565
• Passarge, E., Vogel, F., Berg, K., Bochkov, N. P., Czeizel, A., Emerit, I., Fraccaro, M., Harper, P. S., Ten Kate, L. P., Leroy, J. G., Mikkelsen, M., Norio, R., Rosenkranz, W., Schmid, W., Seemanova, E., & Witkowski, R. (1980). The delivery of genetic counseling services in Europe Human Genetics, 56, 1–5. https://doi.org/10.1007/bf00281565
• Schinzel, A., & Schmid, W. (1980). Interstitial deletion of the long arm of chromosome 1, del(1)(q21-q25) in a profoundly retarded 8-year-old girl with multiple anomalies Clinical Genetics, 18, 305–313. https://doi.org/10.1111/j.1399-0004.1980.tb00890.x
• Schinzel, A. (1980). A case of multiple skeletal anomalies, ectodermal dysplasia, and severe growth and mental retardation Helvetica Paediatrica Acta, 35, 243–251.
• Binkert, F., & Schmid, W. (1980). Influence of vincristine around the time of ovulation and the first cleavage divisions: studies on the karyotype of pre-implantation embryos of Chinese hamsters Mutation Research - Section on Environmental Mutagenesis and Related Subjects, 74, 185–186. https://doi.org/10.1016/0165-1161(80)90035-7
• Schinzel, A. (1980). Trisomy 20pter=q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother Human Genetics, 53, 169–172. https://doi.org/10.1007/bf00273490
• Spranger, J. W., Schinzel, A., Myers, T., Ryan, J., Giedion, A., Opitz, J. M., & Hall, J. G. (1980). Cerebroarthrodigital syndrome: A newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasia American Journal of Medical Genetics, 5, 13–24. https://doi.org/10.1002/ajmg.1320050104
• Schinzel, A. (1980). Klinischer Phänotyp autosomaler Chromosomen-Aberrationene In J. Spranger, J. Gehler, & M. Tolksdorf (Eds.), Klinische Genetik in der Pädiatrie : Symposium (pp. 166–177). Georg Thieme Verlag.
• Schinzel, A., & Schmid, W. (1980). Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: A new syndrome American Journal of Medical Genetics, 6, 241–249. https://doi.org/10.1002/ajmg.1320060308