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. (Q48008172)

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scientific article published in November 1998

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English	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.	scientific article published in November 1998

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6 December 2019

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 (English)

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J C McNaughton

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D J Cockburn

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G Hughes

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W A Jones

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P N Ray

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P A Stockwell

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G B Petersen

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1 November 1998

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6 December 2019

Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene

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

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Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.

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Sequences of junction fragments in the deletion-prone region of the dystrophin gene.

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A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene

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The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene.

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Two hot spots of recombination in the DMD gene correlate with the deletion prone regions

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A transposon-like element in the deletion-prone region of the dystrophin gene

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Identifiers

10.1016/S0378-1119(98)00466-1

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6 December 2019

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