Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing.
about
Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome.Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy.Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults.FBN1 mutations largely contribute to sporadic non-syndromic aortic dissection.Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection.Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing
P2860
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P2860
Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor 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
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@ast
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@en
type
label
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@ast
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@en
prefLabel
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@ast
Rapid molecular genetic diagno ...... y by semiconductor sequencing.
@en
P2093
P2860
P356
P1476
Rapid molecular genetic diagno ...... hy by semiconductor sequencing
@en
P2093
Dao Wen Wang
Dao Wu Wang
Jinzhao Zhao
Zongzhe Li
P2860
P2888
P356
10.1186/1479-5876-12-173
P50
P577
2014-06-17T00:00:00Z
P5875
P6179
1011683229