1. Hereditary familial congenital haemorrhagic nephritis;Alport;Br Med J,1927
2. Alport's syndrome;Andreoli;Ear Nose Throat,1992
3. Waardenburg syndrome (WS): The analysis of a single family with WSI mutation showing linkage to RFLP markers on human chromosome 2q;Asher;Am J Hum Genet,1991
4. Deafness with sporadic goiter: Pendred's syndrome;Batsakis;Arch Otolaryngol,1962
5. The gene for Treacher-Collins syndrome maps to the long arm chromosome 5;Dixon;Am J Hum Genet,1991