A Blankenagel

[Reading aid with a big Fresnel lens for visually handicapped].

W Jaeger, G zu Putlitz, A Blankenagel, 1972, Bericht uber die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft.

[Rand-sight reading aid for visually handicapped--Genensky's cable-television receiver].

W Jaeger, A Blankenagel, F Werner, 1972, Bericht uber die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft.

[Utilization of a new night vision enhancement device (DAVIS)].

K Rohrschneider, A Blankenagel, U Spandau, 2000, Klinische Monatsblatter fur Augenheilkunde.

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.

K Rohrschneider, L I van den Born, M J van Schooneveld, 2001, American journal of human genetics.

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.

K Rohrschneider, A Blankenagel, B. J. Klevering, 1999, American journal of human genetics.

A New Clinical Classification for Usher's Syndrome Based on a New Subtype of Usher's Syndrome Type I

A Blankenagel, W. Kimberling, A. Blankenagel, 2001, The Laryngoscope.

Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt disease.

A Blankenagel, A. Munnich, F. Cremers, 1998, Genomics.

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.

K Rohrschneider, A Blankenagel, A. Deutman, 1998, Human molecular genetics.