1. Association between congenital heart malformation and chromosomal variations;Book, J.A.; Santesson, B.; Zetterqvist, P.;Acta paediat. (Uppsala),1961
2. A family showing transmission of a D/D reciprocal translocation and a case of regular 2i-trisomic Down's syndrome;Cytogenetics,1963
3. Aberrations chromosomiques et maladies humaines-Syndr6me de Klinefelter XXY a 46 chromosomes par fusion centrom6rique T-T;Lejeune, J.; Turpin, R.; DeCourt, J.;C. R. Acad. Sci. (Paris),1960
4. Chromosome preparations of leukocytes cultured from human peripheral blood;Moorhead, P.S.; Nowell, P.C.; Mellman, W.J.; Battips, D.M.; Hungerford, D.A.;Exp. Cell Res,1960
5. Familial transmission of a translocation between two chromosomes of the 13-I5 group (Denver classification);Walker, S.; Harris, R.;Ann. hum. Genet,1962