1989

ZORA Publication List

Publications

• McCormick, M. K., Schinzel, A., Petersen, M. B., Stetten, G., Driscoll, D. J., Cantu, E. S., Tranebjaerg, L., Mikkelsen, M., Watkins, P. C., & Antonarakis, S. E. (1989). Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21. Genomics, 5, 325–331. https://doi.org/10.1016/0888-7543(89)90065-7
• Hammer, J., Kläusler, M., & Schinzel, A. (1989). The popliteal pterygium syndrome: distinct phenotypic variation in two families Helvetica Paediatrica Acta, 43, 507–514.
• Lauener, R., Seger, R., Jörg, W., Hallé, F., Aeppli, R., & Schinzel, A. (1989). Immunodeficiency associated with Dandy–Walker‐like malformation, congenital heart defect, and craniofacial abnormalities American Journal of Medical Genetics, 33, 280–281. https://doi.org/10.1002/ajmg.1320330227
• Schinzel, A. (1989). New and old syndromes American Journal of Medical Genetics, 32, 318–318. https://doi.org/10.1002/ajmg.1320320307
• Gal, A., Schinzel, A., Orth, U., Fraser, N. A., Mollica, F., Craig, I. W., Kruse, T., Mächler, M., Neugebauer, M., & Bleeker-Wagemakers, L. M. (1989). Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp Human Genetics, 81, 315–318. https://doi.org/10.1007/bf00283682
• Hunziker, U. A., Savoldelli, G., Boltshauser, E., Giedion, A., & Schinzel, A. (1989). Prenatal diagnosis of Schwartz–Jampel syndrome with early manifestation Prenatal Diagnosis, 9, 127–131. https://doi.org/10.1002/pd.1970090208
• Boltshauser, E., Stocker, H., & Mächler, M. (1989). Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5) Neurofibromatosis, 2, 244–245.