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The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

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Nature genetics·1994

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European journal of biochemistry·1992

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

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A PvuII polymorphism near exon 2 of the dystrophin gene

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Automating clinically relevant prefetch processes in picture archiving and communication systems solutions.

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q.

RBRVS as a financial assessment tool.

Regulation of expression of a Xenopus borealis embryonic/larval alpha 3 skeletal-actin gene.

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

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

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