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Human Genome Variation|August 10, 2017
The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via <i>POLD1</i> mutation detectionAsami Okada, Tomohiro Kohmoto, Takuya Naruto, et al.Anaerobe|July 10, 2022
First reported case of Lachnoanaerobaculum gingivalis bacteremia in an acute myeloid leukemia patient with oral mucositis during high dose chemotherapyNaoto Okada, Akikazu Murakami, Masami Sato, et al.Journal of Diabetes Investigation|April 9, 2022
Novel method utilizing bisulfite conversion with dual amplification-refractory mutation system polymerase chain reaction to detect circulating pancreatic β-cell cfDNAAsami Okada, Misuzu Yamada-Yamashita, Yukari Tominaga, et al.Pageof 3