Læknablaðið - 01.12.1967, Side 38

238
LÆKNABLAÐIÐ
ÞAKKARORÐ
Við þökkum Dr. J. H. Edwards, Institute of Child Health, Uni-
versity of Birmingham, fyrir litningarannsóknir. Einnig þökkum við
framlag prófessors H. Harris og Dr. E. B. Robson við The Galton La-
boratory, University Collagc, London.
Heimildir
1. Dekaban, A. S. (1966): Transmission of a D/D reciprocal trans-
location in a family with high incidence of mental retardation.
Am. J. of Hum. Gen. 18, 3, 288.
2. Edwards, J. H., Harnden, D. G., Cameron, A. H., Crosse, V. M.
and Wolff, O. H. (1960): A new trisomic syndrome. Lancet 1:
787—790.
3. Huehns, E. R., Lutzner, M. and Hecht, F. (1964): Nuclear abnor-
malities of the neutrofils in Di (13—15) — trisomy syndrome.
Lancet 1: 589.
4. Jacobsen, P., Dupont, A., Mikkelsen, M. (1963): Translocation in
the 13—15 group as a cause of partial trisomy and spontaneous
abortion in the same family. Lancet, i i. 584.
5. Mikkelsen, M. (1966): Transmission of a 13—15 /21 translocation
in six families. Am. J. Hum. Genet. 30, 197.
6. Mikkelsen, M. (1967): DNA replication analysis of six 13—15 /21
translocation families. Am. J. Hum. Genet. 30. 197.
7. Smith, D. W. (1964): Autosomal aþnormalities. Am. J. Obst. &
Gynec. (Symposium on congenital defect). 90, 7, part 2, 1055.
8. Smith, D. W., Patau, K., Therman, E., Inborn, S. L. and De. Mars:
R. I. (1963): The Di trisomy syndrome. Petiatrics, 62, 3, 326.
9. Walker, S., Harris, K. (1962): Investigation of family showing
transmission of a 13—15 chromosomal translocation (Denuer
classification). Brit. Med. J. i i, 25.
10. Walzer, S., Gerald, P. S., Breau, G., O, Neill, D. and Diamond, L.
K (1966): Hematologic chances in the Di trisomy syndrome.
Pediatrics, 38, 3, 419.