Log on / register
Feedback | Support | My details

Comments

Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report

Guillaume de la Houssaye email, Ivan Bieche email, Olivier Roche email, Véronique Vieira email, Ingrid Laurendeau email, Laurence Arbogast email, Hatem Zeghidi email, Philippe Rapp email, Philippe Halimi email, Michel Vidaud email, Jean-Louis Dufier email, Maurice Menasche email and Marc Abitbol email

BMC Medical Genetics 2006, 7:82doi:10.1186/1471-2350-7-82

No comments have yet been made on this article

Post a comment

Terms and Conditions Privacy statement Information for advertisers Jobs at BMC Contact us
© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.