REFERENCES
- Benda, C. E.: Mongolism and Cretinism. New York, Grune & Stratton, Inc., 1946.
- Dunsdon, M.I., Carter, C. O. and Huntley, R. M.: Upper end of range of intelligence in mongolism. Lancet 1: 565, 1960.
- Walker, N. F.: The use of dermal configuration in the diagnosis of mongolism. J. Pediat. 50: 19, 1957.
- Lenz, W.: Angeborene Stoerungen mit abnormer Chromosomenzahl. Schweiz. med. Wchnschr. 90: 1071, 1960.
- Levan, A. and Hsu, T. C.: The human idiogram. Hereditas 45: 665, 1959.
- Lehman, O. and Forssman, H.: Chromosome complement in a mongoloid mother, her child, and the child's father. Lancet 1: 498, 1960.
- Krivit and Good: Cited by Fischler, E. and Farchy, R.: Mongolism associated with acute congenital leukemia. Helvet. paediat. acta 15: 253, 1960.
- Hitzig and Rampini: Cited by Fischler, E. and Farchy, R. Ibid.7
- Hefke, H. W.: Roentgenologic studies of anomalies of the hand in 100 cases of mongolism. Am. J. Dis. Child. 60: 1319, 1940.
- Caffey, J. and Ross, S. T.: Mongolism during early infancy. Pediatrics 17: 642, 1956.
- Caffey, J. and Ross, S. T.: Pelvic bones in infantile mongolism. Am. J. Roentgenol. 80: 458, 1958.
- Annell, A. L.: Incorrect diagnosis of mental deficiency and its consequences. Acta paediat. 32: 95, 1943.
- Doxiades, L. and Portius, w.: Aetiologie des Mongolismus. Ztschr. Menschl. Vererb.-u.Konstitutionslehre 21: 384, 1938.
- Warkany, J.: Etiology of mongolism. J. Pediat. 56: 412, 1960.
- Turpin, R. and Lejeune, J.: Etude d'une famille comportant quatre frères et soeurs mongoliens. Semaine hôp. Paris 29: 3979, 1953.
- Hanhart, E.: Cited by Fanconi, G. and Zellweger, H.: Die bleibenden Schaedigungen des Zentralnervensystems infolge Erkrankungen des Foetusund des Kleinkindes. Schweiz. Arch. Neurol. u. Psychiat. 63: 193, 1949.
- Allen, G. and Baroff, G. S.: Mongoloid twins and their siblings. Acta genet. et statist. 5: 294, 1955.
- Masland, R. L.: Grasp of prenatal influences. Pediat. Herald, October 1960.
- Lenz, W., Nowakowski, H., Prader, A. and Schirren, C.: Die Aetiologie des Klinefelter-Syndroms. Schweiz. med. Wchnschr. 89: 727, 1959.
- Lahdensuu, S.: Ueber Vorkommen und Aetiologie der Idiotia Mongoloidea im Lichte des in Finnland gesammelten Materials. Acta paediat. 21: 256, 1937.
- Witschi, E.: Overripeness of the egg as a cause of twinning and teratogenesis. Cancer Res. 12: 763, 1952.
- Editorial: A proposed standard system of nomenclature of human mitotic chromosomes. Lancet 1: 1063, 1960.
- Ford, E. E., Jacobs, P. A. and Lajtha, L. G.: Human somatic chromosomes. Nature, London 181: 1565, 1958.
- Jacobs, P., Baikie, A. G., Court Brown, W. M. and Strong, J. A.: The somatic chromosomes in mongolism. Lancet 1: 170, 1959.
- Lejeune, J., Turpin, R. and Gautier, M.: Le mongolisme, premier exemple d'aberration autosome humaine. Ann. genet. 1: 41, 1959.
- Stewart, J. S. S. and Stern, C.: Mechanisms of meiotic nondisjunction in man. Nature, London 187: 804, 1960.
- Witschi, E.: Genetic and postgenetic sex determination. Experientia 16: 274, 1960.
- Polani, P., Briggs, J., Ford, C., Clarke, C. and Berg, J.: A mongol girl with 46 chromosomes. Lancet 1: 721, 1960.
- Fraccaro, M., Kaijser, K. and Lindsten, J.: Chromosomal abnormalities in father and mongol child. Ibid.,27 p. 724.
- Böök, J.: Genetic aspects. Acta Soc. med. upsalien. 56: 1, 1960.
- Penrose, L. S., Ellis, J. R. and Delhanty, D. A.: Chromosomal translocation in mongolism and in normal relatives. Lancet 2: 409, 1960.
- Carter, C. O., Hamerton, J. L., Polani, P. E., Gunalp, A. and Weller, S. D. V.: Chromosome translocation as a cause of familial mongolism. Ibid.,30 p. 678.
- Patau, K., Smith, D. w., Therman, E., Inhorn, S. L. and Wagner, H. P.: Multiple congenital anomaly caused by an extra autosome. Lancet 1: 790, 1960.
ADDITIONAL REFERENCES
- Down, J. L. H.: Observations on an ethnic classification of idiots. Clin. Lect. & Rep. London Hospital 3:259, 1866.
- Ingalls, T. H.: Pathogenesis of mongolism. Am. J. Dis. Child. 73:279, 1947.
- Levi, S.: Studio sulla morfologia cerebrale nella idiozia mongoloide. Riv. clin. pediat. 34: 769, 1936.