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Chromosomes and mental retardation1

  • M. Baraitser
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References

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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 Pediatrics 102, 552558.
Edwards, J. H., Harnden, D. G., Cameron, A. H., Crosse, V. M. & Wolff, O. H. (1960). A new trisomic syndrome. Lancet i, 787790.
Fryns, J. P., Jacobs, J., Kleczkowska, A. & van den Berghe, H. (1984). The psychological profile of the fragile X syndrome. Clinical Genetics 25, 131134.
Hunter, A. G. W., Clifford, B. & Cox, D. M. (1985). The characteristic physiognomy and tissue specific karyotype distribution of the Pallister-Killian syndrome. Clinical Genetics 28, 4753.
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 Genetics 27, 113117.
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 Medicine 304, 325329.
Lejeune, J. H. (1959). Le Mongolisme… Premier exemple d'aberration autosomique humaine. Annales de Génetiques 1, 4149.
Lubs, H. A. (1969). A marker X chromosome. American Journal of Human Genetics 21, 231244.
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 Genetics 17, 145157.
Niebuhr, E. (1974). Down syndrome: the possibility of a pathogenetic segement on chromosome no. 21. Humangenetik 21, 99101.
Patau, K., Smith, D. W., Therman, E., Inhorn, S. L. & Wagmer, H. P. (1960). Multiple congential anomaly caused by an extra autosome. Lancet i, 790793.
Sylvester, P. E. (1983). The hippocampus in Down's syndrome. Journal of Mental Deficiency Research 27, 227236.

Chromosomes and mental retardation1

  • M. Baraitser

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