Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.

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Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

@en

Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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P1476

Repeat genetic testing with ta ...... a syndrome and cardiomyopathy.

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Anniek Corveleyn

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Cuno Kuiperi

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Dieter Nuyens

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Erika Souche

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Jeroen Breckpot

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Johan Van Cleemput

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P2860

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A global reference for human genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

ClinVar: public archive of interpretations of clinically relevant variants

Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.

Copy number variation detection and genotyping from exome sequence data.

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing

Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.

P2888

s41431-017-0004-3

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1313-1323

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scholarly article

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10.1038/S41431-017-0004-3

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P478

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2017-10-10T00:00:00Z

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1092152737

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29255176

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5865127

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