Literature DB >> 3464558

Regional localisation of X chromosome short arm probes.

K Paulsen, S Forrest, G Scherer, H H Ropers, K Davies.   

Abstract

Nine human X chromosome-specific clones have been isolated by screening an X-chromosomal genomic library with fetal muscle cDNA. Five of the clones have been localised to the short arm and four to the long arm. The short arm probes have been regionally assigned using a panel of somatic cell hybrids. They have been mapped further using a series of DNA samples from male patients with different deletions of the region Xp21, and having complex phenotypes including Duchenne muscular dystrophy. The use of these probes in the mapping of the short arm of the X chromosome is discussed.

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Year:  1986        PMID: 3464558     DOI: 10.1007/BF00282079

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


  22 in total

1.  Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion.

Authors:  B Wieringa; T Hustinx; J Scheres; W Renier; B ter Haar
Journal:  Clin Genet       Date:  1985-05       Impact factor: 4.438

2.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

3.  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

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

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

5.  Construction and properties of a new cloning vehicle, allowing direct screening for recombinant plasmids.

Authors:  U Rüther
Journal:  Mol Gen Genet       Date:  1980

6.  Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Authors:  A P Read; R V Thakker; K E Davies; R C Mountford; D P Brenton; M Davies; F Glorieux; R Harris; G N Hendy; A King
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

7.  Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Authors:  P Wieacker; K E Davies; H J Cooke; P L Pearson; R Williamson; S Bhattacharya; J Zimmer; H H Ropers
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

Review 8.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

9.  Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry.

Authors:  K E Davies; B D Young; R G Elles; M E Hill; R Williamson
Journal:  Nature       Date:  1981-10-01       Impact factor: 49.962

10.  A glyceraldehyde-3-phosphate dehydrogenase pseudogene on the short arm of the human X chromosomes defines a multigene family.

Authors:  F J Benham; S Hodgkinson; K E Davies
Journal:  EMBO J       Date:  1984-11       Impact factor: 11.598

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  4 in total

1.  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

2.  Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.

Authors:  R J Sinke; B de Leeuw; H A Janssen; D O Weghuis; R F Suijkerbuijk; A M Meloni; S Gilgenkrantz; W Berger; H H Ropers; A A Sandberg
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

3.  Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

Authors:  K E Davies; T J Smith; S Bundey; A P Read; T Flint; M Bell; A Speer
Journal:  J Med Genet       Date:  1988-01       Impact factor: 6.318

4.  Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

Authors:  G de Saint-Basile; M C Bohler; A Fischer; J Cartron; J L Dufier; C Griscelli; S H Orkin
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

  4 in total

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