Doyne revisited

Eye

Volumn 10, Issue 4, 1996, Pages 469-472

  Jay, Marcelle ^a,b   Plant, Catherine ^a   Evans, Kevin ^a   Gregory, Cheryl Y ^a  

^a MOORFIELDS EYE HOSPITAL   (United Kingdom)

^b NONE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLINDNESS; DIFFERENTIAL DIAGNOSIS; FEMALE; GENEALOGY; GENETIC PROCEDURES; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PHENOTYPE; RETINA DEGENERATION; RETINA DYSTROPHY; RETINA MACULA DEGENERATION;

EID: 0029795706     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/eye.1996.103     Document Type: Article

References (10)

1. Doyne RW. Peculiar condition of choroiditis occurring in several members of the same family. Trans Ophthalmol Soc UK 1899;19:71.
2. Doyne RW. A note on family choroiditis. Trans Ophthalmol Soc UK 1910;30:93-5.
3. Mould GT. Family choroiditis. Trans Ophthalmol Soc UK 1910;30:189-90.
4. Doyne RW. Further notes on family choroiditis. Trans Ophthalmol Soc UK 1910;30:274-6.
5. Collins E Treacher. A pathological report upon a case of Doyne's choroiditis ('honeycomb' or 'family' choroiditis). Ophthalmoscope 1913;11:537-8.
6. Foster J. Two cases of ? Doyne's familial choroiditis. Proc R Soc Med 1932;25:990-1.
7. Tree M. Familial hyaline dystrophy in the fundus oculi or Doyne's family honeycomb "choroiditis'. Br J Ophthalmol 1937;21:64-91.
8. Pearce WG. Genetic aspects of Doyne's honeycomb degeneration of the retina. Ann Hum Genet 1967;31:173-87.
9. Pearce WG. Doyne's honeycomb retinal degeneration: clinical and genetic features. Br J Ophthalmol 1968;52:73-8.
10. Dryja TP. Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa. Eye 1992;6:1-10.