Literature DB >> 4800973

Congenital hereditary bilateral non-attachment of retina. A sibship of two.

C I Phillips, D A Leighton, R M Forrester.   

Abstract

Mesh：

Year:  1973        PMID： 4800973     DOI： 10.1111/j.1755-3768.1973.tb06021.x

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


× No keyword cloud information.
  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.  Blindness in schoolchildren: importance of heredity, congenital cataract, and prematurity.

Authors:  C I Phillips; A M Levy; M Newton; N L Stokoe
Journal:  Br J Ophthalmol       Date:  1987-08       Impact factor: 4.638

3.  Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

Authors:  C E van Nouhuys
Journal:  Doc Ophthalmol       Date:  1982-09-23       Impact factor: 2.379

4.  Primary vitreoretinal dysplasia transmitted as an autosomal recessive disorder.

Authors:  N Ohba; S Watanabe; S Fujita
Journal:  Br J Ophthalmol       Date:  1981-09       Impact factor: 4.638

5.  Retinal dysplasia.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-07-15       Impact factor: 2.379

6.  Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.

Authors:  C I Phillips; M Newton; J Duvall; S Holloway; A M Levy
Journal:  Br J Ophthalmol       Date:  1986-04       Impact factor: 4.638
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.