Literature DB >> 3755117

Choroideremia-locus maps between DXS3 and DXS11 on Xq.

A Gal, F Brunsmann, D Hogenkamp, K Rüther, D Ahlert, T F Wienker, W Hammerstein, I H Pawlowitzki.   

Abstract

Choroideremia is a progressive tapetochoroidal dystrophy with X-linked transmission leading frequently to blindness in affected males. The choroideremia-locus (TCD) has recently been assigned to the long arm of the X chromosome by linkage to polymorphic DNA markers. In order to further define the location of the gene defect, two families segregating for choroideremia were examined for DNA restriction fragment length polymorphisms. A search was undertaken for linkage with cloned DNA probes from the proximal short and long arm as well as from the mid-portion of the long arm of the X chromosome. Our data suggest that the most plausible gene order on the Xq is: Xcen-DXYS1-DXS3-TCD-DXS11-Xqter.

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Year:  1986        PMID: 3755117     DOI: 10.1007/bf00291600

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

1.  Choroideremia; clinical and genetic aspects.

Authors:  A SORSBY; A FRANCESCHETTI; R JOSEPH; J B DAVEY
Journal:  Br J Ophthalmol       Date:  1952-10       Impact factor: 4.638

2.  [The fluorescein angiogram in choroidermia (author's transl)].

Authors:  W Hammerstein; E Leide; G Bischof
Journal:  Klin Monbl Augenheilkd       Date:  1977-10       Impact factor: 0.700

3.  Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.

Authors:  P N Goodfellow; K E Davies; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1985

4.  Choroideremia: a clinical and pathologic review.

Authors:  C McCulloch
Journal:  Trans Am Ophthalmol Soc       Date:  1969

5.  Choroideremia and the Xg blood group.

Authors:  A Other
Journal:  Acta Ophthalmol (Copenh)       Date:  1968

6.  Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.

Authors:  D Page; B de Martinville; D Barker; A Wyman; R White; U Francke; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

7.  A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors:  J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

8.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

9.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

10.  X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

Authors:  A Gal; J Mücke; H Theile; P F Wieacker; H H Ropers; T F Wienker
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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  9 in total

1.  Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Authors:  A A Bergen; C Samanns; E J Schuurman; L van Osch; D B van Dorp; A J Pinckers; E Bakker; A Gal; G J van Ommen; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

2.  Linkage studies and deletion screening in choroideremia.

Authors:  A F Wright; R L Nussbaum; S S Bhattacharya; M Jay; J G Lesko; H J Evans; B Jay
Journal:  J Med Genet       Date:  1990-08       Impact factor: 6.318

3.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

4.  Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.

Authors:  S V Hodgson; M E Robertson; C N Fear; J Goodship; S Malcolm; B Jay; M Bobrow; M E Pembrey
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

Review 5.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

6.  Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

Authors:  J G Lesko; R A Lewis; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

7.  Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.

Authors:  M Schwartz; H M Yang; E Niebuhr; T Rosenberg; D C Page
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

8.  Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.

Authors:  D E Merry; J G Lesko; D M Sosnoski; R A Lewis; M Lubinsky; B Trask; G van den Engh; F S Collins; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

9.  Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

Authors:  I M MacDonald; R M Sandre; P Wong; A G Hunter; M P Tenniswood
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

  9 in total

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