首页> 外文OA文献 >P107Prenatal diagnosis of familiar biventricular non-compacted cardiomyopathy with later demonstration of a MYH7 gene mutation

【2h】

P107Prenatal diagnosis of familiar biventricular non-compacted cardiomyopathy with later demonstration of a MYH7 gene mutation

机译：P107熟指诊断熟悉的双心性非压实心肌病，后来证明了一种Myh7基因突变

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
P Guedes Ramallo; L Carrillo Aleman; E Candela Sanchez; E Feliu Rey;
展开▼
作者单位

展开▼
年度 2019
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. GW29-e1531 The Early Diagnosis of MYH7 Gene Mutation Carriers of Hypertrophic Cardiomyopathy Using Multi-Parameter Analysis Model by Conventional 2D- Echocardiography and 3D- Speckle Tracking Imaging [J] . Lisha Na, Dan Zhao, Liwen Liu Journal of the American College of Cardiology . 2018,第16期

机译：GW29-E1531通过常规2D超声心动图和3D-Speckle跟踪成像使用多参数分析模型的肥厚性心肌病的MyH7基因突变载体早期诊断
2. One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations (corrected) in MYH7 rod region. [J] . Hougs L, Havndrup O, Bundgaard H, European journal of human genetics: EJHG . 2005,第2期

机译：丹麦患有MYH7突变的肥厚型心肌病患者中，有三分之一的MYH7杆区具有突变（已校正）。
3. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM [J] . Rani, Deepa Selvi, Nallari, Pratibha, Dhandapany, Perundurai S., DNA and Cell Biology . 2015,第5期

机译：肌节基因的细丝（TPM1）和细丝（MYH7）中双基因突变的共存导致南部印度人FHCM的严重肥厚性心肌病
4. Mutations in the mouse Lmna gene causing progeria, muscular dystrophy and cardiomyopathy [C] . Serguei Kozlov, Leslie Mounkes, Dedra Cutler, Novartis Foundation symposium on Nuclear organization in development and disease . 2005

机译：小鼠LMNA基因中的突变导致普鲁比亚，肌肉营养不良和心肌病
5. Design, Construction, and Verification of a LATE-PCR and Lights-On/Lights-Off Probe Assay for Mutation Detection in Exons 18-21 of the EGFR Gene: Implications for Molecular Diagnosis of Non-Small Cell Lung Carcinoma [D] . Tetrault, Shana Augustin 2012

机译：用于EGFR基因外显子18-21突变检测的LATE-PCR和开/关灯探针检测的设计，构建和验证：对非小细胞肺癌的分子诊断意义
6. Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg→ Trp mutation in exon 13 of the MYH7 gene and a novel mutation 453Arg→ His in exon 14 of the MYH7 gene: A case report [O] . Radovan Haluza, Štěpánka Halouzková, Martin Bunček, 2001

机译：家族性肥厚型心肌病：MYH7基因第13外显子的403Arg→Trp突变和MYH7基因第14外显子的新突变453Arg→His的双重杂合性：病例报告
7. A rare case of familial restrictive cardiomyopathy with mutations in MYH7 and ABCC9 genes [O] . Oana Neagoe, Anda Ciobanu, Rodica Diaconu, 2019

机译：一种罕见的家族式限制性心肌病，具有MyH7和ABCC9基因的突变

P107Prenatal diagnosis of familiar biventricular non-compacted cardiomyopathy with later demonstration of a MYH7 gene mutation

著录项

引文网络

相似文献

相关主题

期刊订阅