Brian P. Brooks
National Eye Institute
National Institutes of Health
Bethesda
MD 20892
USA
Name/email consistency: high
- Analysis of ocular hypopigmentation in Rab38cht/cht mice. Brooks, B.P., Larson, D.M., Chan, C.C., Kjellstrom, S., Smith, R.S., Crawford, M.A., Lamoreux, L., Huizing, M., Hess, R., Jiao, X., Hejtmancik, J.F., Maminishkis, A., John, S.W., Bush, R., Pavan, W.J. Invest. Ophthalmol. Vis. Sci. (2007)
- Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature. Brooks, B.P., Meck, J.M., Haddad, B.R., Bendavid, C., Blain, D., Toretsky, J.A. BMC Med. Genet. (2006)
- Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report. Brooks, B.P., Kleta, R., Caruso, R.C., Stuart, C., Ludlow, J., Stratakis, C.A. BMC. Ophthalmol (2004)
- A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome. Brooks, B.P., Moroi, S.E., Downs, C.A., Wiltse, S., Othman, M.I., Semina, E.V., Richards, J.E. Ophthalmic Genet. (2004)
- Infantile spasms as a cause of acquired perinatal visual loss. Brooks, B.P., Simpson, J.L., Leber, S.M., Robertson, P.L., Archer, S.M. J. AAPOS (2002)