The Evolution of an Intron: Analysis of a Long, Deletion-Prone Intron in the Human Dystrophin Gene

By McNaughton J.C.   Hughes G.   Jones W.A.   Stockwell P.A.   Klamut H.J.   Petersen G.B.  

Genomics, Vol. 40, Iss. 2, 1997-03 ,pp. : 294-304

Academic Press

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Distribution of dystrophin gene deletions mapped by multiplex PCR in the Moravian population

By Fajkusova L.   Kuhrova V.   Hajek J.   Fajkus J.  

Molecular and Cellular Probes, Vol. 11, Iss. 1, 1997-01 ,pp. : 85-87

Academic Press

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Detection of deletion mutations in the hprt gene of T-lymphocytes from healthy and vinylchloride exposed workers by multiplex PCR analysis

By Holzapfel B.   Huttner E.  

Mutation Research/Environmental Mutagenesis and Related Subjects, Vol. 360, Iss. 3, 1996-08 ,pp. : 204-205

Elsevier

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Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene

By McNaughton J.C.   Cockburn D.J.   Hughes G.   Jones W.A.   Laing N.G.   Ray P.N.   Stockwell P.A.   Petersen G.B.  

Gene, Vol. 222, Iss. 1, 1998-11 ,pp. : 41-51

Elsevier

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A new polymorphism in exon 14 of the dystrophin gene detected by RT-PCR and DGGE

By Barbieri A.M.   Soriani N.   Ferrari M.   Carrera P.  

Molecular and Cellular Probes, Vol. 11, Iss. 2, 1997-02 ,pp. : 161-162

Academic Press

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