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Publications by L. Xingyuan

Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

Heart
Cardiovascular MedicineCardiology
2011English

Related publications

Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2011English

Somatic NKX2-5 Mutations as a Novel Mechanism of Disease in Complex Congenital Heart Disease

Journal of Medical Genetics
Genetics
2004English

Novel PITX2c Loss-Of-Function Mutations Associated With Complex Congenital Heart Disease

International Journal of Molecular Medicine
MedicineGenetics
2014English

Congenital Heart Disease

Future Cardiology
Molecular MedicineCardiovascular MedicineCardiology
2012English

Copy Number Variations in the GATA4 , NKX2-5 , TBX5 , BMP4 CRELD1 , and 22q11.2 Gene Regions in Chinese Children With Sporadic Congenital Heart Disease

Journal of Clinical Laboratory Analysis
AllergyImmunologyBiochemistryPublic HealthMedical Laboratory TechnologyClinical BiochemistryHematologyMicrobiologyEnvironmentalOccupational Health
2018English

Advancing Prenatal Detection of Congenital Heart Disease: A Novel Screening Protocol Improves Early Diagnosis of Complex Congenital Heart Disease

Journal of Ultrasound in Medicine
Nuclear MedicineRadiologyUltrasound TechnologyRadiologicalImagingMedicine
2017English

Screening for Fetal Congenital Heart Disease

CMAJ
Medicine
2017English

Cardiac Catheterization for Congenital Heart Disease

2015English

A Mouse Model of Human Congenital Heart Disease: High Incidence of Diverse Cardiac Anomalies and Ventricular Noncompaction Produced by Heterozygous Nkx2-5 Homeodomain Missense Mutation

Circulation: Cardiovascular Genetics
2014English

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