USHERS SYNDROME - WITH SPECIAL REFERENCE TO HETEROZYGOUS MANIFESTATIONS

[11] Franceschetti A, 1963, HEREDO DEGENERESCENC

[12] Frey H, 1904, Z OHRENHEILKD, V48, P331

[13] GEDDA L, 1952, Minerva Med, V43, P433

[14] GEYERMANNERFELT T, 1968, ACVANCES ELECTROPHYS

[15] FAMILIAL ELECTRORETINOGRAPHIC AND ADAPTOMETRIC STUDIES IN RETINITIS PIGMENTOSA [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1958, 46 (03) : 142 - 178

[16] GREINER G F, 1962, Rev Otoneuroophtalmol, V34, P54

[17] GRIMAUD R, 1962, TROUBLES APPAREIL AU

[18] GUERRIER Y, 1960, J FRANC OTORHINOLARY, V9, P1025

[19] HARDY G, 1940, AM J OPHTHALMOL, V23, P315

[20] KARPE G, 1945, ACTA OPHTHAL S24

[11] Franceschetti A, 1963, HEREDO DEGENERESCENC

[12] Frey H, 1904, Z OHRENHEILKD, V48, P331

[13] GEDDA L, 1952, Minerva Med, V43, P433

[14] GEYERMANNERFELT T, 1968, ACVANCES ELECTROPHYS

[15] FAMILIAL ELECTRORETINOGRAPHIC AND ADAPTOMETRIC STUDIES IN RETINITIS PIGMENTOSA [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1958, 46 (03) : 142 - 178

[16] GREINER G F, 1962, Rev Otoneuroophtalmol, V34, P54

[17] GRIMAUD R, 1962, TROUBLES APPAREIL AU

[18] GUERRIER Y, 1960, J FRANC OTORHINOLARY, V9, P1025

[19] HARDY G, 1940, AM J OPHTHALMOL, V23, P315

[20] KARPE G, 1945, ACTA OPHTHAL S24