Literature DB >> 14174213

[TAPETO-RETINAL DEGENERATION OF THE X CHROMOSOME TYPE IN THE NETHERLANDS].

J SCHAPPERT-KIMMIJSER.   

Abstract

Entities:  

Keywords:  CHILD; GENETICS, HUMAN; NETHERLANDS; RETINITIS PIGMENTOSA

Mesh：

Year:  1963        PMID： 14174213

Source DB:  PubMed          Journal:  Bull Mem Soc Fr Ophtalmol        ISSN： 0081-1092


× No keyword cloud information.
  5 in total

1.  X-linked retinitis pigmentosa.

Authors:  A C Bird
Journal:  Br J Ophthalmol       Date:  1975-04       Impact factor: 4.638

2.  Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Authors:  M A Musarella; A Burghes; L Anson-Cartwright; M M Mahtani; R Argonza; L C Tsui; R Worton
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  Usher's syndrome, with special reference to heterozygous manifestations.

Authors:  E B de Haas; G H van Lith; J Rijnders; A M Rümke; C Volmer
Journal:  Doc Ophthalmol       Date:  1970-07-24       Impact factor: 2.379

4.  Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.

Authors:  M A Aldred; K L Dry; E B Knight-Jones; L J Hardwick; P W Teague; D H Lester; J Brown; G Spowart; A D Carothers; J A Raeburn
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

Review 5.  Retinitis pigmentosa and allied diseases: applications of electroretinographic testing.

Authors:  E L Berson
Journal:  Int Ophthalmol       Date:  1981-08       Impact factor: 2.031
  5 in total

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