Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
about
Prenatal findings in patients with prolonged QT interval in the neonatal period.Familial dilated cardiomyopathy.Evidence of a long QT founder gene with varying phenotypic expression in South African families.A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.Arrhythmias in adult congenital heart disease.Normal and abnormal consequences of apoptosis in the human heart: from postnatal morphogenesis to paroxysmal arrhythmiasHereditary dilated cardiomyopathy.Genetics of the long QT syndrome.Congenital disorders of cardiac rhythm and conduction.Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.Long QTc and torsades de pointes in human immunodeficiency virus disease.Increased propensity of women to develop torsades de pointes during complete heart block.Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
P2860
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P2860
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@ast
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@en
type
label
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@ast
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@en
prefLabel
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@ast
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@en
P356
P1433
P1476
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease.
@en
P2093
P304
P356
10.1161/01.CIR.85.6.1973
P407
P577
1992-06-01T00:00:00Z