Chromosomenaberrationen

Albright, S. G., and Hook, E. B.: Estimates of the likelihood that a Down’s syndrome child of unknown genotype is the consequence of an inherited translocation. J. Med. Gent. 17 (1980): 273–276.CrossRefGoogle Scholar

Carr, D. H., and Gedeon, M.: Population cytogenetics of human abortuses. In: Hook, E. B., and Porter, L. M. (Eds.): Population Cytogenetics. Studies in Human Reproduction. Academic Press, New York 1977.Google Scholar

De Grouchy, J., and Turleau, C.: Clinical Atlas of Human Chromosomes. John Wiley, New York 1984.Google Scholar

Ferguson-Smith, M. A.: Prenatal chromosome analysis and its impact on the birth incidence of chromosome disorders. Br. Med. Bull. 39 (1983): 355–364.PubMedGoogle Scholar

Hassold, T., Chan, N., Funkhouser, J. et al.: A cytogenetic study of 1000 spontaneous abortions. Ann. Hum. Genet. 44 (1980): 151–178.PubMedCrossRefGoogle Scholar

Hook, E. B., and Lindsjo, A.: Down syndrome in live birth by single year maternal age interval in a Swedish study. Am. J. Hum. Genet. 30 (1978): 19–27.PubMedGoogle Scholar

ISCN (1978): An International System for Human Cytogenetic Nomenclature (1978). Cytogenet. Cell Genet. 21 (1978): 309–404.CrossRefGoogle Scholar

Jacobs, P. A., Melville, M., Ratcliffe, S., Keay, A. J., and Syme, J.: A cytogenetic survey of 11,680 newborn infants. Ann. Hum. Genet. 37 (1974): 359–376.PubMedCrossRefGoogle Scholar

Lima-de-Faria, A.: Molecular evolution and organization of the chromosome. Elsevier, Amsterdam-New York-Oxford 1983.Google Scholar

Makino, S.: Human Chromosomes. Elsevier, Amsterdam-Oxford 1975.Google Scholar

Mikkelsen, M.: Previous child with Down syndrome and other chromosome aberration. In: Murken, J. D., Stengel-Rutkowski, S., and Schwinger, E. (Eds.): Prenatal Diagnosis. Enke, Stuttgart 1979.Google Scholar

Nagl, W.: Chromosomen. Organisation, Funktion und Evolution des Chromatins. 2. Aufl. Parey, Berlin-Hamburg 1980.Google Scholar

Smith, G. F., and Berg, J. M.: Down’s Anomaly. Churchill Livingstone, London 1976.Google Scholar

Sutherland, G. R., Clisby, S. R., Bloor, G. et al.: Down syndrome in South Australia. Med. J. Aust. 2 (1979): 58–61.PubMedGoogle Scholar

Therman, E.: Human Chromosomes. Springer, New York-Heidelberg-Berlin 1980.CrossRefGoogle Scholar

Young, I. D., Williams, E. M., and Newcombe, R. G.: Down syndrome and maternal age in South Glamorgan. J. Med. Genet. 17 (1980): 433–436.PubMedCrossRefGoogle Scholar

Yunis, J. J.: New Chromosomal Syndromes. Academic Press, New York-San Francisco-London 1979.Google Scholar

Zernahle, K., und Freye, H.-A.: Bedeutung der Chromosomenanalyse in der Humangenetik. Tag.-Ber., Akad. Landwirtsch.-Wiss. DDR, Berlin (1978) 164, 5–15.Google Scholar