References
Conen, P.E. and Erkman, B. (1966). Frequency and occurrence of chromosomal syndromes: D trisomy.Amer. J. Hum. Genet. 18, 374.
Huehn, E.R., Ltzner, M. and Hecht, F. (1964). Nuclear abnormalities of the neutrophils in D (13–15) trisomy syndromeLancet,1, 589.
Marden, P.M., Smith, D.W. and Mac-Donald, M.J. (1964). Congenital anomalies in the newborn by surface examination for anomalies.J. Pediat. 64, 357.
Moorebead, P.S.et al. (1960). Chromosome preparations of leucocytes cultured from human peripheral blood.Exp. Cell Res. 20, 613.
Patau, K.,et al. (1960). Multiple congenital anomalies caused by an extra chromosome.Lancet,1, 790.
Taylor, A.I. (1968). Autosomal trisomy syndromes.J. Med. Genet. 5, 227.
Taylor, M.B., Juberg, R.C., Jones, J. and Johnson, W.A. (1970). Chromosomal variability in the D1 trisomy syndrome.Amer. J. Dis. Child. 120, 374.
Thomson, H. (1965). Abnormalities of autosomal chromosomes.Amer. J. Med. Sci. 250, 718.
Walzer S. (1966). Haematologic changes in the D1 trisomy syndrome,Pediatrics,38, 419.
Yunis, J. J., Hook, E.B. and Mayer, M. (1964). Desoxyribonucleic acid replication pattern of trisomy D.Lancet,2, 935.
Author information
Authors and Affiliations
Additional information
From the Departments of Pathology, Obstetrics and Gynaecology, and Paediatrics, Andhra Medical College, and Victoria Gosha Hospital, Visakhapatnam.
Rights and permissions
About this article
Cite this article
Srinivasa Rao, K., Savithri, C., Ramana Murty, N.V. et al. D1-trisomy syndrome. Indian J Pediatr 41, 22–24 (1974). https://doi.org/10.1007/BF02753582
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02753582