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Publications by Susumu Yonesaka
MYH7 Mutation Identified by Next-Generation Sequencing in Three Infant Siblings With Bi-Ventricular Noncompaction Presenting With Restrictive Hemodynamics
Journal of Cardiology Cases
Cardiovascular Medicine
Cardiology
Clinical and Histopathological Studies in Children With Supraventricular Tachycardia
Japanese Circulation Journal
Related publications
Targeted Next-Generation Sequencing Identified a Novel ANK1 Mutation Associated With Hereditary Spherocytosis in a Chinese Family
Hematology
Hematology
Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing
PLoS ONE
Multidisciplinary
TRPM4 Mutation in Patients With Ventricular Noncompaction and Cardiac Conduction Disease
Circulation. Genomic and precision medicine
Genetics
Cardiovascular Medicine
Cardiology
A Novel Stopgain Mutation c.G992A (p.W331X) in TACR3 Gene Was Identified in Nonobstructive Azoospermia by Targeted Next-Generation Sequencing
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Mutation Scanning in Wheat by Exon Capture and Next-Generation Sequencing
PLoS ONE
Multidisciplinary
A Rare ANOS1 Variant in Siblings With Kallmann Syndrome Identified by Whole Exome Sequencing
Andrology
Endocrinology
Reproductive Medicine
Urology
Metabolism
Diabetes
Distribution Patterns of Segmental Aneuploidies in Human Blastocysts Identified by Next-Generation Sequencing
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
Exome Sequencing Identifies a Mutation in the ACTN2 Gene in a Family With Idiopathic Ventricular Fibrillation, Left Ventricular Noncompaction, and Sudden Death
BMC Medical Genetics
Genetics
GCH1 Heterozygous Mutation Identified by Whole-Exome Sequencing as a Treatable Condition in a Patient Presenting With Progressive Spastic Paraplegia
Journal of Neurology
Neurology
