Literature DB >> 8571973

Nomenclature for inherited diseases of the retina.

C F Inglehearn, A J Hardcastle.   

Abstract

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Mesh：

Year:  1996        PMID： 8571973      PMCID： PMC1914532     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  3 in total

1.  X-linked retinitis pigmentosa.

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

2.  Rod and cone responses in sex-linked retinitis pigmentosa.

Authors:  E L Berson; P Gouras; R D Gunkel; N C Myrianthopoulos
Journal:  Arch Ophthalmol       Date:  1969-02

3.  X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

Authors:  R E McGuire; L S Sullivan; S H Blanton; M W Church; J R Heckenlively; S P Daiger
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025
  3 in total
  2 in total

1.  Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.

Authors:  A J Mears; S Hiriyanna; R Vervoort; B Yashar; L Gieser; S Fahrner; S P Daiger; J R Heckenlively; P A Sieving; A F Wright; A Swaroop
Journal:  Am J Hum Genet       Date:  2000-09-01       Impact factor: 11.025

2.  Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.

Authors:  M Al-Maghtheh; E Vithana; E Tarttelin; M Jay; K Evans; T Moore; S Bhattacharya; C F Inglehearn
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025
  2 in total

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