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TitleAuthors Date of Issue
ミニ染色体を用いた、遺伝子導入のための、ヒト人口染色体ベクターの構築と応用要, 匡; 成富, 研二; 柳, 久美子; Kaname, Tadashi; Naritomi, Kenji; Yanagi, KumikoMar-2005
安定した遺伝子発現の得られるヒト人工染色体の開発と応用要, 匡; 成富, 研二; 柳, 久美子; Kaname, Tadashi; Naritomi, Kenji; Yanagi, KumikoMar-2007
Mild prominence of the Sylvian fissure in a Bainbridge-Ropers syndrome patient with a novel frameshift variant in ASXL3Chinen, Yasutsugu; Nakamura, Sadao; Ganaha, Akira; Hayashi, Shin; Inazawa, Johji; Yanagi, Kumiko; Nakanishi, Koichi; Kaname, Tadashi; Naritomi, KenjiFeb-2018
A novel nonsense SMC1A mutation in a patient with intractable epilepsy and cardiac malformationChinen, Yasutsugu; Nakamura, Sadao; Kaneshi, Takuya; Nakayashiro, Mami; Yanagi, Kumiko; Kaname, Tadashi; Naritomi, Kenji; Nakanishi, Koichi13-May-2019
A novel homozygous missense SLC25A20 mutation in three CACT-deficient patients : clinical and autopsy dataChinen, Yasutsugu; Yanagi, Kumiko; Nakamura, Sadao; Nakayama, Noriko; Kamiya, Motoko; Nakayashiro, Mami; Kaname, Tadashi; Naritomi, Kenji; Nakanishi, Koichi16-Apr-2020

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