Literature DB >> 13184107

[Familial inflammatory pseudoglioma with consanguineous parents].

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Abstract

Keywords:  VITREOUS BODY/diseases

Mesh：

Year:  1954        PMID： 13184107

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  4 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.  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

3.  Retinal dysplasia.

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

4.  Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.

Authors:  Hiroyuki Kondo; Itsuka Matsushita; Tatsuo Nagata; Etsuko Fujihara; Katsuhiro Hosono; Eiichi Uchio; Yoshihiro Hotta; Shunji Kusaka
Journal:  Transl Vis Sci Technol       Date:  2021-06-01       Impact factor: 3.283
  4 in total

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