Keisuke Enomoto

Tokyo, 1138510, Japan

Last Updated: 09/26/2026

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Found 10 publications

Prospective multicenter evaluation of the QuickNavi-Campylobacter assay in stool specimens.

Prospective multicenter evaluation of the QuickNavi-Campylobacter assay in stool specimens.

Journal: Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy

Published: February 26, 2026

Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome.

Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome.

Journal: American journal of medical genetics. Part A

Published: March 26, 2020

Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.

Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.

Journal: Journal of medical genetics

Published: March 18, 2020

Tracheal cartilaginous sleeve in patients with Beare-Stevenson syndrome.

Tracheal cartilaginous sleeve in patients with Beare-Stevenson syndrome.

Journal: Congenital anomalies

Published: March 02, 2019

Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.

Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.

Journal: Clinical epigenetics

Published: December 28, 2018

A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome.

A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome.

Journal: Human genome variation

Published: January 14, 2016

Pure duplication of 19p13.3.

Pure duplication of 19p13.3.

Journal: American journal of medical genetics. Part A

Published: June 10, 2012

Spastic quadriplegia in Down syndrome with congenital duodenal stenosis/atresia.

Spastic quadriplegia in Down syndrome with congenital duodenal stenosis/atresia.

Journal: Congenital anomalies

Published: May 30, 2012

12q14 microdeletion syndrome and short stature with or without relative macrocephaly.

12q14 microdeletion syndrome and short stature with or without relative macrocephaly.

Journal: American journal of medical genetics. Part A

Published: February 06, 2012

Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl.

Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl.

Journal: American journal of medical genetics. Part A

Published: September 28, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026