ALBERT

Schlagwort(e): [abr] AIED; Aland island eye disease ; [abr] CSNB; congential stationary night blindness ; [abr] HR; hereditary retinoschisis ; [abr] OA; ocular albinism ; [abr] OAT; ornithine aminotransferase ; [abr] OED; Oregon eye disease ; [abr] RP; retinitis pigmentosa ; [abr] RS; retinoschisis ; [abr] TCD; tapetochoroidal dystrophy ; [abr] XL; X-linked ; [abr] YAC; yeast artificial chromosome ; [abr] ad; autosomal dominant ; [abr] ar; autosomal recessive

Schlagwort(e): [abr] AIED; Aland island eye disease ; [abr] CSNB; congential stationary night blindness ; [abr] HR; hereditary retinoschisis ; [abr] OA; ocular albinism ; [abr] OAT; ornithine aminotransferase ; [abr] OED; Oregon eye disease ; [abr] RP; retinitis pigmentosa ; [abr] RS; retinoschisis ; [abr] TCD; tapetochoroidal dystrophy ; [abr] XL; X-linked ; [abr] YAC; yeast artificial chromosome ; [abr] ad; autosomal dominant ; [abr] ar; autosomal recessive