The eye in the Marfan syndrome.

Por Maumenee, I H
Publicado em 1981

Colobomatous malformations of the eye.

Por Maumenee, I H, Mitchell, T N
Publicado em 1990

Demonstration of exclusive cilioretinal vascular system supplying the retina in man: vacant discs.

Por Parsa, C F, Cheeseman, E W, Maumenee, I H
Publicado em 1998

The Wagner syndrome versus hereditary arthroophthalmopathy.

Por Maumenee, I H, Stoll, H U, Mets, M B
Publicado em 1982

The ateliotic macula: a newly recognized developmental anomaly.

Por De Pool, M E, el-Hileli, H, Maumenee, I H
Publicado em 2001

A patterned macular dystrophy with yellow plaques and atrophic changes.

Por Cortin, P, Archer, D, Maumenee, I H, Feiock, K, Speros, P
Publicado em 1980

Prevalence of map-dot-fingerprint changes in the cornea.

Por Werblin, T P, Hirst, L W, Stark, W J, Maumenee, I H
Publicado em 1981

Glaucoma in the Marfan syndrome.

Por Izquierdo, N J, Traboulsi, E I, Enger, C, Maumenee, I H
Publicado em 1992

Linkage analysis in dominant optic atrophy.

Por Kivlin, J D, Lovrien, E W, Bishop, D T, Maumenee, I H
Publicado em 1983

Congenital motor nystagmus linked to Xq26-q27.

Por Kerrison, J B, Vagefi, M R, Barmada, M M, Maumenee, I H
Publicado em 1999

Inheritance of congenital esotropia.

Por Maumenee, I H, Alston, A, Mets, M B, Flynn, J T, Mitchell, T N, Beaty, T H
Publicado em 1986

Bilateral symmetry of vision disorders in typical retinitis pigmentosa.

Por Massof, R W, Finkelstein, D, Starr, S J, Kenyon, K R, Fleischman, J A, Maumenee, I H
Publicado em 1979

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretin...

Por Gehrig, A, Felbor, U, Kelsell, R E, Hunt, D M, Maumenee, I H, Weber, B H
Publicado em 1998

Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.

Por Giardiello, F M, Offerhaus, G J, Traboulsi, E I, Graybeal, J C, Maumenee, I H, Krush, A J, Levin, L S, Booker, S V, Hamilton, S R
Publicado em 1991

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Por Sung, C H, Davenport, C M, Hennessey, J C, Maumenee, I H, Jacobson, S G, Heckenlively, J R, Nowakowski, R, Fishman, G, Gouras, P, Nathans, J
Publicado em 1991