O. Camand

Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

C. Orssaud, D. Schorderet, F. Munier, 2006, Molecular vision.

Embryonic expression of the leptin receptor gene in mesoderm-derived tissues.

M. Abitbol, M. Guerre-Millo, S. Turban, 2002, Comptes rendus biologies.

Slit Proteins Regulate Distinct Aspects of Retinal Ganglion Cell Axon Guidance within Dorsal and Ventral Retina

L. Erskine, H. Thompson, O. Camand, 2006, The Journal of Neuroscience.

Mutational analysis of the OA1 gene in ocular albinism

E. Héon, J. Sutherland, J. Dufier, 2003, Ophthalmic genetics.

Mutation analysis of the tyrosinase gene in oculocutaneous albinism

H. Dollfus, E. Héon, J. Sutherland, 2001, Human mutation.

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

P. Czernichow, J. Pantel, S. Amselem, 2001, American journal of human genetics.

Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the “Mowat–Wilson” syndrome

G. Bassez, M. Goossens, M. Catala, 2004, Neurobiology of Disease.