Next-generation sequencing applied to rare diseases genomics.
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Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders.NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.From public health genomics to precision public health: a 20-year journey.
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Next-generation sequencing applied to rare diseases genomics.
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Next-generation sequencing applied to rare diseases genomics.
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Next-generation sequencing applied to rare diseases genomics.
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Next-generation sequencing applied to rare diseases genomics.
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P2093
P2860
P1476
Next-generation sequencing applied to rare diseases genomics.
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P2093
Amanda Lordemann
Cheng-Ho Jimmy Lin
Krissi Danielsson
Liew Jun Mun
P2860
P304
P356
10.1586/14737159.2014.904749
P577
2014-04-04T00:00:00Z