Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology.
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Fetal Magnetic Resonance Imaging of Malformations Associated with HeterotaxyDNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary DyskinesiaDatabases for Congenital Heart Defect Public Health Studies Across the LifespanMMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebratesThrombocytosis in the Setting of Isomerism and a Functionally Univentricular HeartXenopus as a model organism for birth defects-Congenital heart disease and heterotaxyHeterotaxy Syndrome: Proceedings From the 10th International PCICS Meeting.Acute Myocardial Infarction in Adult Congenital Patients with Bodily Isomerism.Cardiac Embryology and Molecular Mechanisms of Congenital Heart Disease: A Primer for Anesthesiologists.Fetal Situs, Isomerism, Heterotaxy Syndrome: Diagnostic Evaluation and Implication for Postnatal Management.Characteristics of Hospitalizations for the Glenn Procedure in Those With Isomerism Compared to Those Without.Practice variability in management of infectious issues in heterotaxy: A survey of pediatric cardiologists.Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways.Racial disparities in heterotaxy syndrome.Claudin5a is required for proper inflation of Kupffer's vesicle lumen and organ laterality.A predictive model of asymmetric morphogenesis from 3D reconstructions of mouse heart looping dynamics.ANKS3 is mutated in a family with autosomal recessive laterality defect.A right-handed signalling pathway drives heart looping in vertebrates.Clinical phenotype and current diagnostic criteria for primary ciliary dyskinesia.Cilia and Ciliopathies in Congenital Heart Disease.A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.Bodily isomerism is an independent risk factor for pulmonary hypertension in adults with congenital heart disease.
P2860
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P2860
Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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name
Laterality defects in the nati ...... and descriptive epidemiology.
@en
Laterality defects in the national birth defects prevention study
@nl
type
label
Laterality defects in the nati ...... and descriptive epidemiology.
@en
Laterality defects in the national birth defects prevention study
@nl
prefLabel
Laterality defects in the nati ...... and descriptive epidemiology.
@en
Laterality defects in the national birth defects prevention study
@nl
P2093
P2860
P356
P1476
Laterality defects in the nati ...... and descriptive epidemiology.
@en
P2093
Angela E Lin
Jaime L Frías
John Belmont
Kelly D Getz
Lorenzo D Botto
Marlene Anderka
Sergey Krikov
P2860
P304
P356
10.1002/AJMG.A.36695
P407
P577
2014-08-06T00:00:00Z