Literature DB >> 3955860

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy.

Y Boyd, V J Buckle.   

Abstract

Lymphoblastoid cell lines have been established from nine female patients with Duchenne muscular dystrophy who had previously been reported to have chromosome translocations with breakpoints in the Xp21 region. A detailed cytogenetic comparison of prometaphase chromosomes in these cell lines revealed that six of the translocations had X chromosome breakpoints in the sub-band Xp212 and that one further breakpoint could be assigned to either Xp212 or Xp213. These findings confirm and extend previous observations and provide strong evidence for Xp212 as the site of the Duchenne and Becker loci. For the remaining two translocations the simplest explanation for the observed banding pattern is that the X chromosome breakpoint lies a few thousand kilobases away, in the sub-band Xp211. Other explanations which assume breaks in Xp212 combined with complex local chromosome rearrangements are also presented. It is also possible that the altered banding pattern in these two cases is due to the influence of local sequences on the staining or uncoiling properties of the chromatin.

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Year:  1986        PMID: 3955860     DOI: 10.1111/j.1399-0004.1986.tb01232.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  26 in total

1.  A familial X;autosome translocation associated with Becker type muscular dystrophy?

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

Review 2.  Improved diagnosis of Duchenne/Becker muscular dystrophy.

Authors:  A H Beggs; L M Kunkel
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

3.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

4.  Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family.

Authors:  Brenna Hayes; Susan Hassed; Jae Lindsay Chaloner; Christopher E Aston; Carrie Guy
Journal:  J Genet Couns       Date:  2015-10-19       Impact factor: 2.537

5.  Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.

Authors:  A P Monaco; C J Bertelson; C Colletti-Feener; L M Kunkel
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

6.  Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.

Authors:  C J Bertelson; J A Bartley; A P Monaco; C Colletti-Feener; K Fischbeck; L M Kunkel
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

7.  Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Authors:  S E Bodrug; J R Roberson; L Weiss; P N Ray; R G Worton; D L Van Dyke
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

Review 8.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

9.  Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus.

Authors:  J A Towbin; D R Wu; J Chamberlain; P D Larsen; W K Seltzer; E R McCabe
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

10.  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

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