242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

Author:

Blonden L.A.J.,Grootscholten P.M.,den Dunnen J.T.,Bakker E.,Abbs S.,Bobrow M.,Boehm C.,van Broeckhoven C.,Baumbach L.,Chamberlain J.,Caskey C.T.,Denton M.,Felicetti L.,Galluzi G.,Fischbeck K.H.,Francke U.,Darras B.,Gilgenkrantz H.,Kaplan J.-C.,Herrmann F.H.,Junien C.,Boileau C.,Liechti-Gallati S.,Lindlöf M.,Matsumoto T.,Niikawa N.,Müller C.R.,Poncin J.,Malcolm S.,Robertson E.,Romeo G.,Covone A.E.,Scheffer H.,Schröder E.,Schwartz M.,Verellen C.,Walker A.,Worton R.,Gillard E.,van Ommen G.J.B.

Publisher

Elsevier BV

Subject

Genetics

Reference29 articles.

1. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies;Baumbach;Neurology,1989

2. High resolution deletion breakpoint mapping in the DMD-gene by whole cosmid hybridization;Blonden;Nucleic Acids Res,1989

3. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) familíes studied with the dystrophin cDNA: Location of breakpoints on HindIII and BgIII exon-containing fragment maps, meiotic and mitotic origin of the mutations;Darras;Am. J. Hum. Genet,1988

4. Direct detection of more than 50% of Duchenne muscular dystrophy mutations by field inversion gels;Den Dunnen;Nature,1987

5. Topography of the DMD gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen;Am. J. Hum. Genet,1989

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