Literature DB >> 11076047

Analysis of dinucleotide repeat loci of dystrophin gene for carrier detection, germline mosaicism and de novo mutations in Duchenne muscular dystrophy.

L S Chaturvedi, R D Mittal, S Srivastava, M Mukherjee, B Mittal.   

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Year:  2000        PMID： 11076047     DOI： 10.1034/j.1399-0004.2000.580312.x

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


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  5 in total

1.  A larger spectrum of intragenic short tandem repeats improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from southern Italy.

Authors:  Antonella Carsana; Giulia Frisso; Maria Roberta Tremolaterra; Elisabetta Ricci; Domenico De Rasmo; Francesco Salvatore
Journal:  J Mol Diagn       Date:  2007-02       Impact factor: 5.568

2.  The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.

Authors:  Veronica Ferreiro; Florencia Giliberto; Liliana Francipane; Irene Szijan
Journal:  Mol Diagn       Date:  2005

3.  Detection of germline mosaicism in two Duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene.

Authors:  Verónica Ferreiro; Irene Szijan; Florencia Giliberto
Journal:  Mol Diagn       Date:  2004

4.  Carrier detection in Duchenne muscular dystrophy using molecular methods.

Authors:  S M Sakthivel Murugan; C Arthi; N Thilothammal; B R Lakshmi
Journal:  Indian J Med Res       Date:  2013-06       Impact factor: 2.375

Review 5.  Muscular dystrophies.

Authors:  Monisha Mukherjee; Balraj Mittal
Journal:  Indian J Pediatr       Date:  2004-02       Impact factor: 5.319
  5 in total

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