Literature DB >> 1351033

Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.

A Cobo1, D Grinberg, S Balcells, L Vilageliu, R Gonzàlez-Duarte, M Baiget.   

Abstract

We used the following polymorphic markers: APOC2 (BanI, BglI, TaqI), CKMM (NcoI, TaqI), and D19S63 (PstI) to haplotype 33 Spanish myotonic dystrophy (DM) families. We analysed the allele and haplotype frequencies of our sample, and the possible association of alleles or haplotypes with the disease. We found a slight linkage disequilibrium between APOC2 (BanI) and DM, but no disequilibrium when using all other APOC2 and CKMM RFLPs; this agrees with data previously reported. In addition, we found a very strong linkage disequilibrium when using D19S63 (PstI), the + allele being associated with the DM locus. This disequilibrium in the Spanish population indicates that D19S63 is very close to the DM locus.

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Year:  1992        PMID: 1351033     DOI: 10.1007/bf00220541

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


  25 in total

1.  A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119).

Authors:  R G Korneluk; C Tsilfidis; G Shutler; M Mahadevan; J Bailly; L C Surh
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

2.  Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.

Authors:  C Lavedan; C Duros; D Savoy; S Leblond; J Bailly; R Korneluk; C Junien
Journal:  Genomics       Date:  1990-12       Impact factor: 5.736

3.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

4.  Identification of new DNA markers close to the myotonic dystrophy locus.

Authors:  J D Brook; H G Harley; K V Walsh; S A Rundle; M J Siciliano; P S Harper; D J Shaw
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

5.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

6.  Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.

Authors:  K Johnson; P Shelbourne; J Davies; J Buxton; E Nimmo; M Anvret; M Bonduelle; B Williamson; M L Savontaus
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

7.  A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.

Authors:  R G Korneluk; H L MacLeod; T W McKeithan; J D Brooks; A E MacKenzie
Journal:  Genomics       Date:  1989-02       Impact factor: 5.736

8.  Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Authors:  H G Brunner; R G Korneluk; M Coerwinkel-Driessen; A MacKenzie; H Smeets; H M Lambermon; B A van Oost; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

9.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

Review 10.  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

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  2 in total

1.  Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Authors:  A Goldman; A Krause; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

2.  French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.

Authors:  C Lavedan; H Hofmann-Radvanyi; C Boileau; C Bonaïti-Pellié; D Savoy; P Shelbourne; C Duros; J P Rabes; I Dehaupas; S Luce
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

  2 in total

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