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Publications by Andrassi, M

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Jump to: 2000 | 1999
Number of items: 2.

2000

Krämer, F, White, K, Pauleikhoff, D, Gehrig, A, Passmore, L, Rivera, A, Rudolph, G, Kellner, U, Andrassi, M, Lorenz, B, Rohrschneider, K, Blankenagel, A, Jurklies, B, Schilling, H, Schütt, F, Holz, F G and Weber, Bernhard H. F. (2000) Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics 8 (4), pp. 286-292. Fulltext not available.

1999

Gehrig, A, Lorenz, B, Andrassi, M and Weber, Bernhard H. F. (1999) First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis. Journal of Medical Genetics 36 (12), pp. 933-934. Fulltext not available.

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