1. Le diagnostic prenatal des anomalies genetiques;Boue, A.;Concoiurs Medical,1977
2. Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1;Garver, K.L.; Ciocco, A.M.; Turack, N.A.;Clinical Genetics,1976
3. Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46, XY, del(l)(q25q32);Koivisto, M.; Akerblom, H.K.; Remes, M.; de la Chapelle, A.;Acta Paediatrica Scandinavica,1976
4. A partial trisomy of chromosome 1 in a family with a t(lq-; 4q+) translocation;Neu, R.L.; Gardner, L.I.;Clinical Genetics,1973
5. Trisomy of the long arm of human chromosome 1;Norwood, T.H.; Hoehn, H.;Humangenetik,1974