Noriko M. Sangu
Tokyo, Japan
Last Updated: 09/26/2026
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Found 20 publications
Mandibular Fracture in a Patient Taking a Direct Oral Anticoagulant.
Journal: The Journal of craniofacial surgery
Published: October 10, 2020
A 7q31.33q32.1 microdeletion including LRRC4 and GRM8 is associated with severe intellectual disability and characteristics of autism.
Journal: Human genome variation
Published: June 21, 2016
A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene.
Journal: Human genome variation
Published: March 07, 2016
7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly.
Journal: European journal of medical genetics
Published: November 02, 2015
Use of targeted next-generation sequencing for molecular diagnosis of craniosynostosis: Identification of a novel de novo mutation of EFNB1.
Journal: Congenital anomalies
Published: April 19, 2015
Characteristics of patients with benign partial epilepsy in infancy without PRRT2 mutations.
Journal: Epilepsy research
Published: April 10, 2015
Leukoencephalopathy associated with 11q24 deletion involving the gene encoding hepatic and glial cell adhesion molecule in two patients.
Journal: European journal of medical genetics
Published: February 08, 2015
Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
Journal: Brain & development
Published: September 29, 2014
An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation.
Journal: American journal of medical genetics. Part A
Published: April 29, 2014
Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
Journal: Brain & development
Published: April 02, 2014
Last Updated: 09/26/2026