A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis.

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Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.Array comparative genomic hybridization identifies a heterozygous deletion of exon 3 of the RYR2 gene

P2860

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P2860

A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis.

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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P1476

A Streamlined Protocol for Mol ...... directional Sequence Analysis.

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Chuan-Ching Lan

http://www.w3.org/2001/XMLSchema#string

Daniel Lai

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Donald R Love

http://www.w3.org/2001/XMLSchema#string

Jennifer M Love

http://www.w3.org/2001/XMLSchema#string

Renate Marquis-Nicholson

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P2860

Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing

A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies.

X-linked dilated cardiomyopathy and the dystrophin gene.

Rapid direct sequence analysis of the dystrophin gene

Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.

Array-based Identification of Copy Number Changes in a Diagnostic Setting: Simultaneous gene-focused and low resolution whole human genome analysis.

Microarray-based mutation detection in the dystrophin gene.

Genetics of Duchenne muscular dystrophy.

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scholarly article

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10.1155/2013/908317

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2013

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2013-02-07T00:00:00Z

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A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis.

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P2860

P2860

A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis.

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P2860

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P932