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Publications by Jing‑Yi Hou
TBX1 Loss‑of‑function Mutation Contributes to Congenital Conotruncal Defects
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Related publications
COL6A1 Loss of Function Mutation Underlie Atrioventricular Septal Defects in Down Syndrome Patients
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
Mutation Analysis of TBX1 in Non-Deleted Patients With Features of DGS/VCFS or Isolated Cardiovascular Defects
Journal of Medical Genetics
Genetics
Evaluation of Heterogeneity in the Association Between Congenital Heart Defects and Variants of Folate Metabolism Genes: Conotruncal and Left-Sided Cardiac Defects
Birth Defects Research Part A - Clinical and Molecular Teratology
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology
Gain-Of-Function Mutation in Gli3 Causes Ventricular Septal Defects
Comprehensive Approach to Congenital Heart Defects
Journal of Cardiovascular Disease Research
Cardiovascular Medicine
Cardiology
Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients With Congenital Hypopituitarism
PLoS ONE
Multidisciplinary
Loss of NEIL1 Causes Defects in Olfactory Function in Mice
Neurobiology of Aging
Aging
Gerontology
Developmental Biology
Geriatrics
Neuroscience
Neurology
A Human De Novo Mutation inMYH10phenocopies the Loss of Function Mutation in Mice
Rare Diseases
