Literature DB >> 2239970

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

M Coleman1, S Bhattacharya, S Lindsay, A Wright, M Jay, M Litt, I Craig, K Davies.   

Abstract

The microsatellite marker DXS426 maps to the interval Xp21.1-Xp11.21, the chromosomal region which contains two loci for X-linked retinitis pigmentosa (XLRP; RP2 and RP3). We have refined the localization of DXS426 both physically, by mapping it to a deletion which spans the interval Xp21.3-Xp11.23, and genetically, by studying multiply informative crossovers which indicate that DXS426 lies between DXS7 and DXS255 (i.e., Xp11.4-Xp11.22). As this is the region which contains the RP2 gene, RP2 families could be identified on the basis of linkage of XLRP to DXS426. Multiply informative crossovers in two RP2 families indicate that the most likely location of the RP2 gene is between DXS426 and DXS7. DXS426 is therefore an important highly informative marker for the purposes of carrier detection and early diagnosis of RP2 and for the localization of the disease gene.

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Year:  1990        PMID: 2239970      PMCID: PMC1683909     

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


  21 in total

1.  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

2.  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

3.  Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.

Authors:  L M Kunkel; U Tantravahi; M Eisenhard; S A Latt
Journal:  Nucleic Acids Res       Date:  1982-03-11       Impact factor: 16.971

4.  A modified ERG technique and the results obtained in X-linked retinitis pigmentosa.

Authors:  G B Arden; R M Carter; C R Hogg; D J Powell; W J Ernst; G M Clover; A L Lyness; M P Quinlan
Journal:  Br J Ophthalmol       Date:  1983-07       Impact factor: 4.638

5.  Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

Authors:  C Ingle; R Williamson; A de la Chapelle; R R Herva; K Haapala; G Bates; H F Willard; P Pearson; K E Davies
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

6.  Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.

Authors:  S S Bhattacharya; A F Wright; J F Clayton; W H Price; C I Phillips; C M McKeown; M Jay; A C Bird; P L Pearson; E M Southern
Journal:  Nature       Date:  1984 May 17-23       Impact factor: 49.962

7.  Simple sequences are ubiquitous repetitive components of eukaryotic genomes.

Authors:  D Tautz; M Renz
Journal:  Nucleic Acids Res       Date:  1984-05-25       Impact factor: 16.971

8.  DNA probes in X-linked retinitis pigmentosa.

Authors:  A F Wright; S Bhattacharya; W H Price; C I Phillips; C McKeown; S J Crews; M Jay; A C Bird
Journal:  Trans Ophthalmol Soc U K       Date:  1983

9.  Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease.

Authors:  A Gal; B Wieringa; D F Smeets; L Bleeker-Wagemakers; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1986

10.  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

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  14 in total

1.  Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Authors:  L Strain; A F Wright; D T Bonthron
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Prenatal exclusion of Norrie's disease.

Authors:  R M Redmond; C A Graham; E D Kelly; M Coleman; N C Nevin
Journal:  Br J Ophthalmol       Date:  1992-08       Impact factor: 4.638

3.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

4.  X-linked retinitis pigmentosa: new map studies of XLRP2, and a possible human centromere effect.

Authors:  U Friedrich; M Warburg; T A Kruse; S Andréasson
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

5.  A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Authors:  R Fujita; E Bingham; P Forsythe; C McHenry; V Aita; B A Navia; K Dry; M Segal; M Devoto; G Bruns; A F Wright; J Ott; P A Sieving; A Swaroop
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

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

Authors:  S Lindsay; D L Thiselton; J B Bateman; J T Ngo; R S Sparkes; M Coleman; K E Davies; S S Bhattacharya
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

7.  Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Authors:  A F Wright; S S Bhattacharya; M A Aldred; M Jay; A D Carothers; N S Thomas; A C Bird; B Jay; H J Evans
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

8.  A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.

Authors:  C U Kirchgessner; J A Trofatter; M M Mahtani; H F Willard; L J DeGennaro
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

9.  Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).

Authors:  H K Hong; R E Ferrell; M B Gorin
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

10.  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

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