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Publications by Andrassi, M

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


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.


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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