Literature DB >> 13889236

Familial retinal detachment.

J EDMUND.   

Abstract

Entities:  

Keywords:  RETINAL DETACHMENT/genetics

Mesh:

Year:  1961        PMID: 13889236     DOI: 10.1111/j.1755-3768.1961.tb00279.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


× No keyword cloud information.
  6 in total

1.  Lattice degeneration in a family: with retinal detachment and cataract.

Authors:  I Lewkonia; M S Davies; J D Salmon
Journal:  Br J Ophthalmol       Date:  1973-08       Impact factor: 4.638

Review 2.  The Wagner-Stickler syndrome complex.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-12-16       Impact factor: 2.379

3.  Syndromes of genetic juvenile retinal detachment.

Authors:  R J Gorlin; W H Knobloch
Journal:  Z Kinderheilkd       Date:  1972

4.  COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.

Authors:  A J Richards; S Martin; J R Yates; J D Scott; D M Baguley; F M Pope; M P Snead
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

5.  Inherited hyaloideoretinopathy and skeletal dysplasia.

Authors:  W H Knobloch
Journal:  Trans Am Ophthalmol Soc       Date:  1975

6.  Autosomal dominant juvenile vitreoretinal degeneration and retinal detachment.

Authors:  K M Saari
Journal:  Int Ophthalmol       Date:  1986-04       Impact factor: 2.031

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.