Literature DB >> 5026847

Linkage studies in X-linked retinitis pigmentosa.

P Grützner, R Sanger, B E Spivey.   

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Year:  1972        PMID： 5026847     DOI： 10.1007/BF00273301

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  3 in total

1.  Chorioretinal degeneration or retinitis pigmentosa of intermediate sex-linked heredity.

Authors:  J FRANCOIS
Journal:  Doc Ophthalmol       Date:  1962       Impact factor: 2.379

2.  X-linked retinitis pigmentosa and linkage studies with the Xg blood-groups.

Authors:  D Klein; A Franceschetti; I Hussels; R R Race; R Sanger
Journal:  Lancet       Date:  1967-05-06       Impact factor: 79.321

3.  Sex-linked recessive retinitis pigmentosa. A preliminary study of the carriers.

Authors:  M Warburg; S E Simonsen
Journal:  Acta Ophthalmol (Copenh)       Date:  1968
  3 in total
  5 in total

1.  Linkage studies of typical retinitis pigmentosa and common markers.

Authors:  I Hussels-Maumenee; E R Pierce; W B Bias; D A Schleutermann
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

2.  Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.

Authors:  M A Spence; R S Sparkes; J R Heckenlively; J T Pearlman; D Zedalis; M Sparkes; M Crist; S Tideman
Journal:  Am J Hum Genet       Date:  1977-07       Impact factor: 11.025

3.  X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Authors:  U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers.

Authors:  R L Nussbaum; R A Lewis; J G Lesko; R Ferrell
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Authors:  U Francke; H D Ochs; B de Martinville; J Giacalone; V Lindgren; C Distèche; R A Pagon; M H Hofker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025
  5 in total

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