Literature DB >> 1733838

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.

S Lindsay1, D L Thiselton, J B Bateman, J T Ngo, R S Sparkes, M Coleman, K E Davies, S S Bhattacharya.   

Abstract

A highly informative microsatellite marker, DXS426, which maps proximal to DXS7 in the interval Xp11.4-Xp11.23, has been used to refine further the localisation of the gene for Norrie disease (NDP). The results from a multiply informative crossover localize the NDP gene proximal to DXS7. In conjunction with information from 2 NDP patients who have a deletion for DXS7 but not for DSX426, our data indicate that the NDP gene lies between DXS7 and DXS426 on proximal Xp.

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Year:  1992        PMID： 1733838     DOI： 10.1007/bf00197273

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


  16 in total

1.  Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

Authors:  M Coleman; S Bhattacharya; S Lindsay; A Wright; M Jay; M Litt; I Craig; K Davies
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  Dinucleotide repeat polymorphism at the MAOA locus.

Authors:  G C Black; Z Y Chen; I W Craig; J F Powell
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

3.  Genetic and physical mapping around the properdin P gene.

Authors:  M P Coleman; J C Murray; H F Willard; K F Nolan; K B Reid; D J Blake; S Lindsay; S S Bhattacharya; A Wright; K E Davies
Journal:  Genomics       Date:  1991-12       Impact factor: 5.736

4.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Authors:  R K Saiki; S Scharf; F Faloona; K B Mullis; G T Horn; H A Erlich; N Arnheim
Journal:  Science       Date:  1985-12-20       Impact factor: 47.728

5.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

6.  Further linkage data on Norrie disease.

Authors:  J D Kivlin; G E Sanborn; E Wright; L Cannon; J Carey
Journal:  Am J Med Genet       Date:  1987-03

7.  Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

Authors:  G I Bell; J H Karam; W J Rutter
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

8.  Physical fine-mapping of a deletion spanning the Norrie gene.

Authors:  P J Diergaarde; B Wieringa; E M Bleeker-Wagemakers; K B Sims; X O Breakefield; H H Ropers
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

9.  Norrie disease resulting from a gene deletion: clinical features and DNA studies.

Authors:  D Donnai; R C Mountford; A P Read
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

10.  Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Authors:  L M Bleeker-Wagemakers; U Friedrich; A Gal; T F Wienker; M Warburg; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
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  1 in total

1.  Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Authors:  S J Scheinman; M A Pook; C Wooding; J T Pang; P A Frymoyer; R V Thakker
Journal:  J Clin Invest       Date:  1993-06       Impact factor: 14.808
  1 in total

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