PAX6 references

Ann Neurol 2003 May;53(5):658-63
Polymicrogyria and absence of pineal gland due to PAX6 mutation.
Mitchell TN, Free SL, Williamson KA, Stevens JM, Churchill AJ, Hanson IM, Shorvon SD, Moore AT, van Heyningen V, Sisodiya SM

Pax6 (Associated with Aniridia and Limbal Stem Cell Deficiency) http://www.theocularsurface.com/V1N1-Kao.htm

heyman I. Frampton I. Van Heyingen V et al. Psychiatric disorder and cognitive function in a famility with inherited novel mutation of the developmental control gene pax6 Psychiatr genet 199: 9: 85-90

Molecular and Cellular Probes (1997) 11, 287 292 Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations. R. A. Axton, I. M. Hanson, J. Love, A. Seawright, J. Prosser and V. van Heyningen, (Received 14 May 1997, Accepted 9 June 1997)1997 Academic Press Limited
 
J Med Genet 1996 Jan;33(1):66-8 
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13). Crolla JA, Cross I, Atkey N, Wright M, Oley, CA.

Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)9p13q12.2)] Hum Genet 1986 v. 72, 297-302 Moore J.W. et al