Literature DB >> 13662558

Episkopi blindness; hereditary blindness in a Greek Cypriot family.

P J TAYLOR, T COATES, M L NEWHOUSE.   

Abstract

Entities:  

Keywords:  BLINDNESS/heredity

Mesh:

Year:  1959        PMID: 13662558      PMCID: PMC512223          DOI: 10.1136/bjo.43.6.340

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


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  6 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Bilateral Norrie's disease in identical twins.

Authors:  K Sukumaran
Journal:  Br J Ophthalmol       Date:  1991-03       Impact factor: 4.638

3.  Norrie's disease in an Asian family.

Authors:  D G Harendra de Silva; D B de Silva
Journal:  Br J Ophthalmol       Date:  1988-01       Impact factor: 4.638

4.  [Incidence of primary band-shaped corneal dystrophy, other degenerative corneal lesions, and keratoconus in a family (author's transl)].

Authors:  W Lisch
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1974

5.  X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

Authors:  A E Krill
Journal:  Trans Am Ophthalmol Soc       Date:  1969

6.  Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

Authors:  G Wolff; A Mayerová; T F Wienker; P Atalianis; P Ioannou; M Warburg
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

  6 in total

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