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Publications by Yohei Matsuzaki
A Neonatal Case of HDR Syndrome and a Vascular Ring With a Novel GATA3 Mutation
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Gene Expression and Biological Processes Influenced by Deletion of Stat3 in Pulmonary Type II Epithelial Cells
BMC Genomics
Biotechnology
Genetics
Related publications
A Rare Cause of Primary Hypoparathyroidism Due to a Novel Mutation in the GATA3 Gene – The Barakat Syndrome
International Journal of Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Case of Allgrove Syndrome With a Novel IVS7 +1 G>A Mutation of the AAAS Gene
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel Site Mutation in a Wiskott-Aldrich Syndrome Boy: A Case Report
Biomedical Journal of Scientific & Technical Research
A Novel Gene Mutation in Berardinelli Seip Syndrome: Three Case Reports
Endocrine Abstracts
A Novel TRPS1 Mutation in a Moroccan Family With Tricho-Rhino-Phalangeal Syndrome Type III: Case Report
BMC Medical Genetics
Genetics
A Novel Mutation in a Kazakh Family With X-Linked Alport Syndrome
PLoS ONE
Multidisciplinary
A Recurring FBN1 Gene Mutation in Neonatal Marfan Syndrome
Archives of Pediatrics & Adolescent Medicine
A Novel Missense Mutation of COL5A2 in a Patient With Ehlers–Danlos Syndrome
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Identification of a Novel Nonsense Mutation in SH2D1A in a Patient With X-Linked Lymphoproliferative Syndrome Type 1: A Case Report
BMC Medical Genetics
Genetics
