1979

ZORA Publication List

Publications

• Schinzel, A. A. G. L., Smith, D. W., & Miller, J. R. (1979). Monozygotic twinning and structural defects Journal of Pediatrics, 95, 921–930. https://doi.org/10.1016/s0022-3476(79)80278-4
• Schinzel, A. (1979). The Coffin-Siris syndrome Acta Paediatrica, 68, 449–452. https://doi.org/10.1111/j.1651-2227.1979.tb05037.x
• Schinzel, A. (1979). Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome? Helvetica Paediatrica Acta, 34, 141–146.
• Binkert, F., & Schmid, W. (1979). Comparison between dominant-lethal curve and karyotypes of preimplantation embryos in Chinese hamster up to 10 weeks after a single dose of an alkylating mutagen Mutation Research - Section on Environmental Mutagenesis and Related Subjects, 64, 116–117. https://doi.org/10.1016/0165-1161(79)90030-x
• Schinzel, A. (1979). Fetales Hydantoin-Syndrom bei Geschwistern Schweizerische Medizinische Wochenschrift, 109, 68–72.
• Binkert, F., & Schmid, W. (1979). Swiss Society for Genetics. Abstracts of previously unpublished presentations given at the annual meeting on June 9, 1979 in Schwerzenbach Archiv Für Genetik, 51, 243–249.
• Schinzel, A. (1979). Possible trisomy 1q25→1q32 in a malformed girl with a de novo insertion in 1q Human Genetics, 49, 167–173. https://doi.org/10.1007/bf00277638
• Goor, W., Maier, C., Fierz, W., Otte, F., Pedio, G., Rüttner, J. R., & Schmid, W. (1979). The Sézary Syndrome Dermatologica, 158, 397–403. https://doi.org/10.1159/000250789
• Schmid, W. (1979). Trisomy for the distal third of the long arm of chromosome 19 in brother and sister Human Genetics, 46, 263–270. https://doi.org/10.1007/bf00273309
• Schinzel, A. (1979). Der neuen Terminus Sonderpädagogik, 9, 142–143.
• Schinzel, A., & Tönz, O. (1979). Partial trisomy 7q and probable partial monosomy of 5p in the son of a mother with a reciprocal translocation between 5p and 7q Human Genetics, 53, 121–124. https://doi.org/10.1007/bf00289464
• Miller, M., Kaufman, G., Reed, G., Bilenker, R., & Schinzel, A. (1979). Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 → 7p21 American Journal of Medical Genetics, 4, 323–332. https://doi.org/10.1002/ajmg.1320040403
• Schmid, W., D’Apuzzo, V., & Rossi, E. (1979). Trisomy 6q25→6qter in a severely retarded 7-year-old boy with turricephaly, bow-shaped mouth, hypogenitalism and club feet Human Genetics, 46, 279–284. https://doi.org/10.1007/bf00273311
• Schinzel, A. (1979). Trisomy 9p, a Chromosome Aberration with Distinct Radiologic Findings Radiology, 130, 125–133. https://doi.org/10.1148/130.1.125