Literature DB >> 2882476

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

M Patterson, S Kenwrick, S Thibodeau, K Faulk, M G Mattei, J F Mattei, K E Davies.   

Abstract

We report the identification of a new RFLP detected by the DNA probe MN12, which is linked to both the fragile site on the X chromosome at Xq27.3 and the highly polymorphic locus detected by St14 (DXS52). In situ mapping confirms the localisation of MN12 distal to the fragile site. A detailed physical analysis of this region of the X chromosome using pulsed-field gel electrophoresis has shown that MN12, St14 and DX13 (DXS15) are physically linked within a region of 470kb. A long range restriction map around the MN12 locus reveals at least two candidate HTF islands, suggesting the existence of expressed sequences in this region.

Entities:  

Mesh:

Year:  1987        PMID: 2882476      PMCID: PMC340674          DOI: 10.1093/nar/15.6.2639

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  17 in total

1.  Long-range restriction site mapping of mammalian genomic DNA.

Authors:  W R Brown; A P Bird
Journal:  Nature       Date:  1986 Jul 31-Aug 6       Impact factor: 49.962

2.  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

3.  The marker (X) syndrome: a cytogenetic and genetic analysis.

Authors:  S L Sherman; N E Morton; P A Jacobs; G Turner
Journal:  Ann Hum Genet       Date:  1984-01       Impact factor: 1.670

4.  Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2, and 9.

Authors:  D A Laurie; M Hultén; G H Jones
Journal:  Cytogenet Cell Genet       Date:  1981

Review 5.  Marker (X)-linked mental retardation.

Authors:  G Turner; P Jacobs
Journal:  Adv Hum Genet       Date:  1983

6.  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

7.  Long-range restriction map around the Duchenne muscular dystrophy gene.

Authors:  M Burmeister; H Lehrach
Journal:  Nature       Date:  1986 Dec 11-17       Impact factor: 49.962

8.  Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis.

Authors:  D C Schwartz; C R Cantor
Journal:  Cell       Date:  1984-05       Impact factor: 41.582

9.  Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.

Authors:  K E Davies; P L Pearson; P S Harper; J M Murray; T O'Brien; M Sarfarazi; R Williamson
Journal:  Nucleic Acids Res       Date:  1983-04-25       Impact factor: 16.971

10.  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

View more
  24 in total

1.  Adrenoleucodystrophy: a molecular genetic study in five families.

Authors:  R G Del Mastro; S Bundey; M W Kilpatrick
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors:  M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

Review 3.  The fragile X: progress toward solving the puzzle.

Authors:  W T Brown
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

4.  Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Authors:  R Feil; G Palmieri; M d'Urso; R Heilig; I Oberlé; J L Mandel
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

5.  Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.

Authors:  M A Voelckel; M G Mattei; C N'Guyen; N Philip; F Birg; J F Mattei
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

6.  Physical mapping of DXS134 close to the DXS52 locus.

Authors:  M V Bell; M N Patterson; H R Dorkins; K E Davies
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

7.  Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.

Authors:  M A Voelckel; N Philip; C Piquet; M C Pellissier; I Oberlé; F Birg; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

8.  A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Authors:  A Vincent; C Kretz; I Oberlé; J L Mandel
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

9.  Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.

Authors:  A Sefiani; R M'rad; L Simard; A Vincent; C Julier; L Holvoet-Vermaut; S Heuertz; N Dahl; J F Stalder; M O Peter
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

10.  Rapid screening of a human genomic library in yeast artificial chromosomes for single-copy sequences.

Authors:  C N Traver; S Klapholz; R W Hyman; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.