The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome
about
The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.Monogenic disorders that mimic the phenotype of Rett syndrome.MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
P2860
The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome
description
2015 nî lūn-bûn
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2015 թուականին հրատարակուած գիտական յօդուած
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2015 թվականին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
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name
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@ast
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@en
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@nl
type
label
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@ast
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@en
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@nl
prefLabel
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@ast
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@en
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@nl
P2860
P356
P1476
The Utility of Next-Generation ...... ve Patients with Rett Syndrome
@en
P2093
Wendy Anne Gold
P2860
P356
10.3389/FNCEL.2015.00266
P407
P577
2015-07-14T00:00:00Z