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International Journal of Hematology|December 17, 2024
Chimerism analysis by ABO blood group genotyping with digital droplet PCRTakuya Naruto, Maiko Sagisaka, Mieko Ito, et al.Cancer Chemotherapy and Pharmacology|October 15, 2013
Flow cytometric chemosensitivity assay using JC‑1, a sensor of mitochondrial transmembrane potential, in acute leukemiaTomoko Yokosuka, Hiroaki Goto, Hisaki Fujii, et al.Journal of Human Genetics|August 16, 2018
Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletionYukiko Kuroda, Ikuko Ohashi, Takuya Naruto, et al.Plos One|November 7, 2015
Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin SyndromeKei-ichi Morita, Takuya Naruto, Kousuke Tanimoto, et al.Human Genome Variation|April 16, 2016
A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndromeTomohiro Kohmoto, Atsumi Tsuji, Kei-Ichi Morita, et al.European Journal of Medical Genetics|January 3, 2019
CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disabilityYumi Enomoto, Yoshinori Tsurusaki, Takayuki Yokoi, et al.Human Genome Variation|November 22, 2016
Exome-first approach identified a novel gloss deletion associated with Lowe syndromeMiki Watanabe, Ryuji Nakagawa, Tomohiro Kohmoto, et al.Journal of Virology|April 23, 2010
Long-term control of HIV-1 in hemophiliacs carrying slow-progressing allele HLA-B*5101Yuka Kawashima, Nozomi Kuse, Hiroyuki Gatanaga, et al.Human Genome Variation|April 22, 2017
Detection of 1p36 deletion by clinical exome-first diagnostic approachMiki Watanabe, Yasunobu Hayabuchi, Akemi Ono, et al.Journal of the Neurological Sciences|April 23, 2017
Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasiaMikako Enokizono, Noriko Aida, Tetsu Niwa, et al.Pageof 11