We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Dobyns, W. B., Stratton, R. F., Parke, J. T., Greenberg, F., Nussbaum, R. L. & Ledbetter, D. H. (1983). Miller-Dieker syndrome and monosomy 17p. Journal of Pediatrics102, 552–558.CrossRefGoogle ScholarPubMed
Edwards, J. H., Harnden, D. G., Cameron, A. H., Crosse, V. M. & Wolff, O. H. (1960). A new trisomic syndrome. Lanceti, 787–790.CrossRefGoogle Scholar
Fryns, J. P., Jacobs, J., Kleczkowska, A. & van den Berghe, H. (1984). The psychological profile of the fragile X syndrome. Clinical Genetics25, 131–134.CrossRefGoogle ScholarPubMed
Hunter, A. G. W., Clifford, B. & Cox, D. M. (1985). The characteristic physiognomy and tissue specific karyotype distribution of the Pallister-Killian syndrome. Clinical Genetics28, 47–53.CrossRefGoogle ScholarPubMed
K:son Blomquist, H., Bohman, M., Edvinsson, S. O., Gillberg, C., Gustavson, K.-H., Holmgren, G. & Wahlstróm, J. (1985). Frequency of the fragile X syndrome in infantile autism. A Swedish multicentre study. Clinical Genetics27, 113–117.CrossRefGoogle Scholar
Ledbetter, D. H., Riccardi, V., Airhart, S. D., Strobel, R. J., Keenan, B. S. & Crawford, J. D. (1981). Deletions of chromosome 15 as a cause of Prader-Willi Syndrome. New England Journal of Medicine304, 325–329.CrossRefGoogle ScholarPubMed
Lejeune, J. H. (1959). Le Mongolisme… Premier exemple d'aberration autosomique humaine. Annales de Génetiques1, 41–49.Google Scholar
Lubs, H. A. (1969). A marker X chromosome. American Journal of Human Genetics21, 231–244.Google ScholarPubMed
Lubs, H. A., Travers, H., Lujan, E. & Carroll, A. (1984). A large kindred with X-linked mental retardation, marker X and macroorchidism. American Journal of Medical Genetics17, 145–157.CrossRefGoogle Scholar
Niebuhr, E. (1974). Down syndrome: the possibility of a pathogenetic segement on chromosome no. 21. Humangenetik21, 99–101.Google Scholar
Patau, K., Smith, D. W., Therman, E., Inhorn, S. L. & Wagmer, H. P. (1960). Multiple congential anomaly caused by an extra autosome. Lanceti, 790–793.CrossRefGoogle Scholar
Sylvester, P. E. (1983). The hippocampus in Down's syndrome. Journal of Mental Deficiency Research27, 227–236.Google ScholarPubMed