This is a preview of subscription content, log in via an institution to check access.
Literatur
Breibart, S., W. J. Mellman, and W. R. Eberlein: Developmental retardation associated with an unbalanced 13–15/18 translocation. Cytogenetics 3, 252–257 (1964).
Bridges, C. B.: Deficiency. Genetics 2, 445 (1917).
Bühler, E. M., U. K. Bühler, and G. R. Stalder: Partial monosomy 18 and anomaly of thyroxine synthesis. Lancet 1964/I, 170–171.
German, J.L., J. Lejeune, M. N. Macintyre, and J. de Grouchy: Chromosomal autoradiography in the cri-du-chat-syndrome. Cytogenetics 3, 347–352 (1964).
Gustavson, K. H., S. C. Finley, W. H. Finley, and B. Jalling: A 4–5/21–22 chromosomal translocation associated with multiple congenital anomalies. Acta paediat. (Uppsala) 53, 172–181 (1964).
Hirschhorn, K., and H. L. Cooper: Apparent deletion of short arms of one chromosome (4 or 5) in a child with defects of midline fusion. Human Chromos. Nwsl. 4, 14 (1961) und als persönliche Mitteilung bei: M. W. Shaw, M. M. Cohen, and H. M. Hildebrandt: A familial 4/5 reciprocal translocation resulting in partial trisomy B. Amer. J. hum. Genet. 1, 54–70 (1965).
Lejeune, J., J. Lafourcade, R. Berger et R. Turpin: Ségrégation familiale d'un translocation 5/13 déterminant une monosomie et une trisomie partielles du bras court du chromosome 5: Maladie du “Cri du chat” et sa “reciproke”. C. R. Acad. Sci. (Paris) 258, 5767 (1964).
—, J. Vialatte, M. Boeswillwald, P. Seringe et R. Turpin: Trois cas de délétion partielle du bras court d'un chromosome 5. C. R. Acad. Sci. (Paris) 257, 3098 (1963).
Moorhead, P. S., P. C. Nowell, W. J. Mellman, D. M. Battips and D. A. Hungerford: Chromosome preparations of leucocytes cultured from human peripheral blood. Exp. Cell. Res. 20, 613–616 (1960).
Ohno, S., W. Beçak, and M. L. Beçak: X-autosome ratio and the behaviour pattern of individual X-chromosomes in placental mammals. Chromosoma (Berl.) 15, 14–30 (1964).
Pätau, K.: Identification of chromosomes. In: Human Chromosome Methodology (J. J. Yunis, Ed.), p. 155–186. New York-London: Academic Press 1965.
Penrose, L. S.: Dermatoglyphics in mosaic mongolism and allied conditions. Genetics Today. Proc. XI Int. Congr. Genet., The Hague 1963, Vol. 3, p. 973. Pergamon Press 1965.
Rieger, R., u. A. Michaelis: Genetisches und Cytogenetisches Wörterbuch, S. 648. Berlin-Göttingen-Heidelberg: Springer 1958.
Schmid, W.: DNA replication patterns of human chromosomes. Cytogenetics 2, 175–193 (1963).
Stalder, G. R., E. M. Bühler u. U. K. Bühler: Nachkommen von balancierten fusions-und translokations-heterzygoten Menschen. Helv. paediat. Acta 20, 169–184 (1965).
Summitt, R. L.: Deletion of the short arm of Chromosome 18. Cytogenetics 3, 201–206 (1964).
Therman, E., K. Patau, R. J. de Mars, D. W. Smith, and S. L. Inhorn: Iso/Telo D1 mocaicism in a child with an incomplete D1 trisomy syndrome. Port. Acta biol. A 7, 211–224 (1963).
van Dyke, H. E., A. Valdmanis, and J. D. Mann: Probable deletion of the short arm of chromosome 18. Amer. J. hum. Genet. 3, 364–374 (1964).
White, P. R.: The cultivation of animal and plant cells, p. 109. New York: Ronald Press 1954.
Author information
Authors and Affiliations
Additional information
Wesentliche Teile der vorliegenden Arbeit werden von Fräulein Renate Porsch als Dissertation der Medizinischen Fakultät der Universität Freiburg i. Br. vorgelegt.
Rights and permissions
About this article
Cite this article
Wolf, U., Reinwein, H., Porsch, R. et al. Defizienz an den kurzen Armen eines Chromosomes Nr. 4. Hum Genet 1, 397–413 (1965). https://doi.org/10.1007/BF00279119
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00279119