Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Fengwen Liao
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
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Related publications
Novel NKX2-5 Mutations Responsible for Congenital Heart Disease
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
The Importance of Copy Number Variation in Congenital Heart Disease
npj Genomic Medicine
Genetics
Molecular Biology
Novel NKX2-5 Mutations Responsible for Congenital Heart Disease
Heart
Cardiovascular Medicine
Cardiology
Copy Number Variation in Congenital Heart Defects
Current Genetic Medicine Reports
Somatic NKX2-5 Mutations as a Novel Mechanism of Disease in Complex Congenital Heart Disease
Journal of Medical Genetics
Genetics
Analysis of Germline Gene Copy Number Variants of Patients With Sporadic Pancreatic Adenocarcinoma Reveals Specific Variations
Oncology
Medicine
Cancer Research
Oncology
No Evidence for Mosaic Pathogenic Copy Number Variations in Cardiac Tissue From Patients With Congenital Heart Malformations
European Journal of Medical Genetics
Medicine
Genetics
Contribution of Congenital Heart Disease to Neuropsychiatric Outcome in School-Age Children With 22q11.2 Deletion Syndrome
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
Psychiatry
Molecular Neuroscience
Mental Health
Genetics
Cellular
Genetic Variations of ISL1 Associated With Human Congenital Heart Disease in Chinese Han People
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
