Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophies

Author:

Fassati Ariberto,Tedeschi Silvana,Bordoni Andreina,Amboni Paolo,Curcio Cristina,Bresolin Nereo,Scarlato Guglielmo

Publisher

Elsevier BV

Subject

General Medicine

Reference10 articles.

1. Duchenne muscular dystrophy;Emery,1993

2. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen;Am J Hum Genet,1989

3. Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene;Abbs;Genomics,1990

4. Analysis of cytokine mRNA: detection and quantitation by competitive polymerase chain reaction;Gilliland;Proc Natl Acad Sci USA,1990

5. Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy;Roberts;Nucleic Acids Res,1989

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1. Detection of dystrophin deletion carriers using FISH analysis;Clinical Genetics;2008-06-28

2. D;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

3. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination;Prenatal Diagnosis;2005

4. Duchenne muscular dystrophy: hopes for the sesquicentenary;Medical Journal of Australia;2003-11

5. Restriction Fragment Length Polymorphisms (RFLPs);Wiley Encyclopedia of Molecular Medicine;2002-01-15

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