A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
about
A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases.TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosusAn update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.HAND2 Target Gene Regulatory Networks Control Atrioventricular Canal and Cardiac Valve Development.MEF2C loss-of-function mutation contributes to congenital heart defects.TBX1 loss-of-function mutation contributes to congenital conotruncal defects.HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.Distinct epigenomic patterns are associated with haploinsufficiency and predict risk genes of developmental disorders.
P2860
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P2860
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@ast
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@en
type
label
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@ast
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@en
prefLabel
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@ast
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@en
P2093
P2860
P356
P1433
P1476
A HAND2 Loss-of-Function Mutat ...... Defect and Pulmonary Stenosis.
@en
P2093
Hong-Yu Shi
Ri-Tai Huang
Xin-Kai Qu
Xing-Biao Qiu
Xu-Min Hou
Yi-Qing Yang
P2860
P304
P356
10.1534/G3.115.026518
P577
2016-02-10T00:00:00Z