1. The fragile X syndrome;Fryns;A study of 83 families. Clin. Genet.,1984
2. DNA polymerase a inhibition by aphi-dicolin induces gaps and breaks at common fragile sites in human chromosomes.;Glover;Hum. Genet.,1984
3. Aspects génétiques des sites fragiles autosomiques. A propos de 40 cas.;Guichaoua;J. Génét. Hum.,1982
4. International Workshop on Human Gene Mapping, Los Angeles.;Human Gene Mapping VII;Cyogenet. Cell Genet.,1983
5. Lacune stéréotypée constitutionelle des chromosomes humains.;Quack;J. Génét. Hum.,1978