Literature DB >> 6094335

The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers.

T C Gilliam, P Scambler, T Robbins, C Ingle, R Williamson, K E Davies.   

Abstract

A library of DNA sequences cloned in lambda phage has been prepared from DNA of chromosomes sorted by cytofluorimetry to give enrichment for chromosome 4. Five sequences have been assigned to chromosome 4 using a panel of hybrid cells, and each has been localised relative to a translocation breakpoint at 4q26. Each of the probes gives a Southern blot pattern which indicates that it does not cross-hybridize with sequences found on other human chromosomes. Three of the probes reveal frequent restriction fragment length polymorphisms (RFLPs) and are useful for linkage analysis.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6094335     DOI: 10.1007/bf00279306

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


  22 in total

1.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

2.  Precise identification of various chromosomal abnormalities.

Authors:  K Hirschhorn; M Lucas; I Wallace
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

3.  A new method for the preparation of metaphase chromosomes for flow analysis.

Authors:  R Sillar; B D Young
Journal:  J Histochem Cytochem       Date:  1981-01       Impact factor: 2.479

4.  Somatic cell genetic studies of the cystic fibrosis mucociliary inhibitor.

Authors:  B J Mayo; R J Klebe; D R Barnett; B J Lankford; B H Bowman
Journal:  Clin Genet       Date:  1980-11       Impact factor: 4.438

5.  A polymorphic DNA marker genetically linked to Huntington's disease.

Authors:  J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal:  Nature       Date:  1983 Nov 17-23       Impact factor: 49.962

6.  Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.

Authors:  J C Murray; C M Demopulos; R M Lawn; A G Motulsky
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

7.  Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNA.

Authors:  P Humphries; D Barton; A M McKay; M M Humphries; B Carritt
Journal:  Mol Gen Genet       Date:  1983

Review 8.  The application of DNA recombinant technology to the analysis of the human genome and genetic disease.

Authors:  K E Davies
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 9.  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

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.  Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes.

Authors:  T G Lugo; B Handelin; A M Killary; D E Housman; R E Fournier
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

2.  Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Authors:  C E Schwartz; J P Johnson; B Holycross; T M Mandeville; T S Sears; E A Graul; J C Carey; R J Schroer; M C Phelan; J Szollar
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

3.  A RFLP for A56 (D5S) an anonymous DNA sequence from chromosome 5.

Authors:  P J Scambler; R Williamson
Journal:  Nucleic Acids Res       Date:  1985-09-25       Impact factor: 16.971

4.  The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4.

Authors:  M Farrall; P Scambler; P North; R Williamson
Journal:  Am J Hum Genet       Date:  1986-01       Impact factor: 11.025

5.  Re: Savtchenko et al. (1988): "Embryonic Expression of the Human 40-kD Keratin: Evidence from a Processed Pseudogene Sequence".

Authors:  C E Boklage
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

6.  An anonymous clone E9pl (D4S112) localised to 4q26-qter detects an Msp I RFLP.

Authors:  T P Robbins; P J Scambler; K E Davies; R Williamson
Journal:  Nucleic Acids Res       Date:  1987-10-12       Impact factor: 16.971

7.  The parental origin and mechanism of formation of three dicentric X chromosomes.

Authors:  M C Phelan; L A Prouty; R E Stevenson; P N Howard-Peebles; D C Page; C E Schwartz
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

8.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

9.  Microdissection of and microcloning from the short arm of human chromosome 2.

Authors:  G P Bates; B J Wainwright; R Williamson; S D Brown
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

10.  Exclusion of the Friedreich ataxia gene from chromosome 19.

Authors:  S Chamberlain; C S Worrall; S South; J Shaw; M Farrall; R Williamson
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.