Whole-exome sequencing identifies novel SGCD and ACVRL1 mutations associated with Total Anomalous Pu

来源 :第六届亚太儿科心脏协会年会 | 被引量 : 0次 | 上传用户：lsssyd

【作者】

：

Shiwei Yang Jun Li Zhening Pu Junchen Dai Tao Jiang Fangzhi Du Yue Chen Genyin Dai Jun Wang Cong Ren Liming Cao Xueying Cheng Yuming Qin

【机构】

：

Department of Cardiology,Nanjing Children Nanjing 210008

【出处】

：

第六届亚太儿科心脏协会年会

【发表日期】

：

2016年3期

下载到本地 , 更方便阅读

下载此文赞助VIP

声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架

论文部分内容阅读

其他文献

以面神经麻痹为首发症状的川崎病一例

会议

Effect of Gordon model case management training on nursing quality in department of Children Interve

会议

Immune function examination and clinical significance in children with Endocardial fibroelastosis

Objective: The purpose of the study was to summarize the characteristics of cellular and humoral immunity in children with Endocardial fibroelastosis(EFE),and to explore the role of cellular and humor

会议

Endocardial fibroelastosisT-lymphocyte subsetsB-lymphocytesIVIG

The change of serum and urine electrolytes in children with neurally mediated syncope after oral reh

会议

Klf13 as a novel collaborator of Gata5 in Bicuspid aortic valve formation

会议

The study of motor performance in congenital heart disease

会议

Study on association of single nucleotide polymorphism of β1 adrenergic receptor gene with right ven

会议

The circadian rhythm of neurally mediated syncope--Singlecenter study

会议

Phosphorylation of Src(Tyr 416)Kinase,ErbB2(Y878)and Myofilament Tyrosines are upregulated in R92Q T

会议

Targeted next-generation sequencing(NGS)of 22 candidate genes in congenital heart disease patients w

会议

Whole-exome sequencing identifies novel SGCD and ACVRL1 mutations associated with Total Anomalous Pu

与本文相关的学术论文