Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients

Author:

Dinçer Pervin,Topalogˇlu Haluk,Ayter Şükrüye,Özgüç Meral,Tas¸demir Haydar Ali,Renda Yavuz

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Normal human genomic restriction fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA;Darras;Am J Hum Genet,1988

2. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987

3. 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

4. Deletion screening of the DMD locus via multiplex DNA amplification;Chamberlain;Nucleic Acids Res,1988

5. Multiplex PCR for the diagnosis of DMD;Chamberlain,1990

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