Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Embedding in Epoxy Resins for Ultrathin Sectioning in Electron Microscopy

1960 • 3,319 citations

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 • 1,051 citations

Purkinje cell degeneration, a new neurological mutation in the mouse.

1976 • 595 citations

Genetics and Probability in Animal Breeding Experiments

1981 • 425 citations

Usher syndrome: Definition and estimate of prevalence from two high-risk populations

1983 • 367 citations

RETINAL DEGENERATION IN THE MOUSE

1965 • 288 citations

Fat (fat) and Tubby (tub): Two Autosomal Recessive Mutations Causing Obesity Syndromes in the Mouse

1990 • 270 citations

Localization of two genes for usher syndrome type I to chromosome 11

1992 • 221 citations

Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains

1993 • 218 citations

Localization of Usher syndrome type II to chromosome 1q

1990 • 217 citations

A New H‐2‐Linked Mutation, rds, Causing Retinal Degeneration in the Mouse

1978 • 192 citations

Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11

1992 • 185 citations

Clinical Findings and Common Symptoms in Retinitis Pigmentosa

1988 • 168 citations

Usher's Syndrome

1983 • 148 citations

Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q

1990 • 137 citations

Comparative map for mice and humans

1992 • 133 citations

New Mouse Primary Retinal Degeneration (rd-3)

1993 • 112 citations

Usher's Syndrome Type III

1979 • 53 citations

Histopathology of the Inner Ear in Usher's Syndrome as Observed by Light and Electron Microscopy

1986 • 38 citations

9. Retinitis Pigmentosa

1981 • 34 citations

Screening for mouse retinal degenerations

1989 • 30 citations

Screening for mouse retinal degenerations

1989 • 4 citations