Literature DB >> 2881880

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

U Friedrich, H Brunner, D Smeets, E Lambermon, H H Ropers.   

Abstract

In seven large families with myotonic dystrophy (DM) comprising 102 individuals, linkage studies were performed employing restriction fragment length polymorphisms in the complement component 3 gene and the 19cen C banding heteromorphism as genetic markers. Three-point linkage analysis excludes DM from the 19cen-C3 segment and strongly supports its assignment to the proximal long arm of chromosome 19.

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Year:  1987        PMID： 2881880     DOI： 10.1007/bf00281077

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


  9 in total

1.  Estimation of linkage between the Lutheran and the Lewis blood groups.

Authors:  J MOHR
Journal:  Acta Pathol Microbiol Scand       Date:  1951

2.  Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.

Authors:  T Hulsebos; B Wieringa; R Hochstenbach; D Smeets; J Schepens; F Oerlemans; J Zimmer; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1986

3.  Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19.

Authors:  S Naylor; J M Lalouel; D J Shaw
Journal:  Cytogenet Cell Genet       Date:  1985

4.  Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

Authors:  J H Renwick; S E Bundey; M A Ferguson-Smith; M M Izatt
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

5.  Genetic linkage between the loci for myotonic dystrophy and peptidase D.

Authors:  T O'Brien; S Ball; M Sarfarazi; P S Harper; E B Robson
Journal:  Ann Hum Genet       Date:  1983-05       Impact factor: 1.670

6.  Centromere heteromorphism in chromosome 19.

Authors:  U Friedrich
Journal:  Clin Genet       Date:  1985-10       Impact factor: 4.438

7.  RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).

Authors:  A D Roses; M A Pericak-Vance; D A Ross; L Yamaoka; R J Bartlett
Journal:  Nucleic Acids Res       Date:  1986-07-11       Impact factor: 16.971

8.  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

9.  Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.

Authors:  H Eiberg; J Mohr; L S Nielsen; N Simonsen
Journal:  Clin Genet       Date:  1983-09       Impact factor: 4.438
  9 in total
  10 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments.

Authors:  J D Brook; S J Knight; S H Roberts; H G Harley; K V Walsh; S A Rundle; K Freyne; M C Koch; N D Epstein; B Wieringa
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

Review 3.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Authors:  H J Smeets; H G Brunner; H H Ropers; B Wieringa
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

5.  The genes for CD37, CD53, and R2, all members of a novel gene family, are located on different chromosomes.

Authors:  K I Virtaneva; P Angelisová; T Baumruker; V Horejsí; H Nevanlinna; J Schröder
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

6.  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

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

Authors:  A Cobo; D Grinberg; S Balcells; L Vilageliu; R Gonzàlez-Duarte; M Baiget
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

8.  Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Authors:  B Smeets; J Poddighe; H Brunner; H H Ropers; B Wieringa
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

9.  Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair.

Authors:  R L Stallings; E Olson; A W Strauss; L H Thompson; L L Bachinski; M J Siciliano
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

10.  Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Authors:  K V Walsh; H G Harley; J D Brook; S A Rundle; M Sarfarazi; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132
  10 in total

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