Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing
about
Medical implications of technical accuracy in genome sequencingUse of contemporary genetics in cardiovascular diagnosisA 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseasesParent and public interest in whole-genome sequencingEmergency medical genomes: a breakthrough application of precision medicine.Early somatic mosaicism is a rare cause of long-QT syndrome.Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence.Genetics of long-QT syndrome.A primer to clinical genome sequencingThe Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long QT Syndrome.The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
P2860
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P2860
Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@ast
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@en
type
label
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@ast
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@en
prefLabel
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@ast
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@en
P2093
P2860
P1433
P1476
Molecular diagnosis of long QT ...... rapid whole genome sequencing
@en
P2093
Anne M Dubin
Euan A Ashley
Frederick E Dewey
James R Priest
Katsuhide Maeda
Lindsey E Malloy-Walton
Marco V Perez
Scott R Ceresnak
P2860
P304
P356
10.1016/J.HRTHM.2014.06.030
P577
2014-06-25T00:00:00Z