CLUTCH COVER von ADACHI, NAOMICHI

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FOUR-WHEEL-DRIVE VEHICLE von ADACHI NAOMICHI

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Clutch cover von ADACHI, NAOMICHI

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Differential gear apparatus with worm gears von ADACHI, NAOMICHI, NAKAO, TOSHIYUKI

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TORQUE TRANSMITTING DEVICE FOR AUTOMOBILE von ADACHI NAOMICHI, ONO HIROKI

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TORSIONAL VIBRATION ABSORBING DEVICE von ADACHI NAOMICHI, ISHIDA NOBUYASU

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DAMPER DISC von ADACHI NAOMICHI, TAKI SHUICHI

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CLUTCH RELEASE BEARING DEVICE von ADACHI NAOMICHI, BAN HIROSHI

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JP2841549B von ARAKAWA YOSHIFUMI, ADACHI NAOMICHI, KOBAYASHI YASUHIRO

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Detecting a long insertion variant in SAMD12 by SMRT sequencing: implications of long-read whole-genome sequencing for repeat expansion diseases von Mizuguchi, Takeshi, Toyota, Tomoko, Adachi, Hiroaki, Miyake, Noriko, Matsumoto, Naomichi, Miyatake, Satoko

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Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads von Mitsuhashi, Satomi, Frith, Martin C, Mizuguchi, Takeshi, Miyatake, Satoko, Toyota, Tomoko, Adachi, Hiroaki, Oma, Yoko, Kino, Yoshihiro, Mitsuhashi, Hiroaki, Matsumoto, Naomichi

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Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures von Takahashi, Yuji, Date, Hidetoshi, Oi, Hideki, Adachi, Takeya, Imanishi, Noriaki, Kimura, En, Takizawa, Hotake, Kosugi, Shinji, Matsumoto, Naomichi, Kosaki, Kenjiro, Matsubara, Yoichi, Ando, Yukio, Anzai, Toshihisa, Ariga, Tadashi, Fukushima, Yoshimitsu, Furusawa, Yoshihiko, Ganaha, Akira, Goto, Yuichi, Hata, Kenichiro, Honda, Masataka, Iijima, Kazumoto, Ikka, Tsunakuni, Imoto, Issei, Kaname, Tadashi, Kobayashi, Masao, Kojima, Seiji, Kurahashi, Hiroki, Kure, Shigeo, Kurosawa, Kenji, Maegaki, Yoshihiro, Makita, Yoshio, Morio, Tomohiro, Narita, Ichiei, Nomura, Fumio, Ogata, Tsutomu, Ozono, Keiichi, Oka, Akira, Okamoto, Nobuhiko, Saitoh, Shinji, Sakurai, Akihiro, Takada, Fumio, Takahashi, Tsutomu, Tamaoka, Akira, Umezawa, Akihiro, Yachie, Akihiro, Yoshiura, Kouichiro, Chinen, Yasutsugu, Eguchi, Mariko, Fujio, Keishi, Hosoda, Kiminori, Ichikawa, Tomohiko, Kawarai, Toshitaka, Kosho, Tomoki, Masuno, Mitsuo, Nakamura, Akie, Nakane, Takaya, Ogi, Tomoo, Okada, Satoshi, Sakata, Yasushi, Seto, Toshiyuki, Takahashi, Yoshiyuki, Takano, Tadao, Ueda, Mitsuharu, Yagasaki, Hideaki, Yamamoto, Toshiyuki, Watanabe, Atsushi, Hotta, Yoshihiro, Kubo, Akiharu, Maruyama, Hirofumi, Moriyama, Keiji, Nanba, Eiji, Sakai, Norio, Sekijima, Yoshiki, Shimosegawa, Toru, Takeuchi, Tsutomu, Usami, Shinichi, Yamamoto, Kazuhiko, Mizusawa, Hidehiro

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Clinical course of epilepsy and white matter abnormality linked to a novel DYRK1A variant von Okazaki, Tetsuya, Yamada, Hiroyuki, Matsuura, Kaori, Kasagi, Noriko, Miyake, Noriko, Matsumoto, Naomichi, Adachi, Kaori, Nanba, Eiji, Maegaki, Yoshihiro

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Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic CBL Variant von Tatsuya Kawaguchi, Tohru Okanishi, Tetsuya Okazaki, Chisako Aoki, Noriko Kasagi, Kaori Adachi, Yuichi Yoshida, Noriko Miyake, Naomichi Matsumoto, Yoshihiro Maegaki

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Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion von Okazaki, Tetsuya, Kawaguchi, Tatsuya, Saiki, Yusuke, Aoki, Chisako, Kasagi, Noriko, Adachi, Kaori, Saida, Ken, Matsumoto, Naomichi, Nanba, Eiji, Maegaki, Yoshihiro

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Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations von Kohashi, Kosuke, Ishiyama, Akihiko, Yuasa, Shota, Tanaka, Tomomi, Miya, Kazushi, Adachi, Yuichi, Sato, Noriko, Saitsu, Hirotomo, Ohba, Chihiro, Matsumoto, Naomichi, Murakami, Yoshiko, Kinoshita, Taroh, Sugai, Kenji, Sasaki, Masayuki

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Cost Evaluation of CRF-Based Bibliography Extraction from Reference Strings von Kawakami, Naomichi, Ohta, Manabu, Takasu, Atsuhiro, Adachi, Jun

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Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation von Mizuguchi, Takeshi, Toyota, Tomoko, Koshimizu, Eriko, Kameyama, Shinichi, Fukuda, Hiromi, Tsuchida, Naomi, Uchiyama, Yuri, Hamanaka, Kohei, Fujita, Atsushi, Misawa, Kazuharu, Miyatake, Satoko, Adachi, Hiroaki, Matsumoto, Naomichi

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Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencing von Hijikata, Atsushi, Suyama, Mikita, Kikugawa, Shingo, Matoba, Ryo, Naruto, Takuya, Enomoto, Yumi, Kurosawa, Kenji, Harada, Naoki, Yanagi, Kumiko, Kaname, Tadashi, Miyako, Keisuke, Takazawa, Masaki, Sasai, Hideo, Hosokawa, Junichi, Itoga, Sakae, Yamaguchi, Tomomi, Kosho, Tomoki, Matsubara, Keiko, Kuroki, Yoko, Fukami, Maki, Adachi, Kaori, Nanba, Eiji, Tsuchida, Naomi, Uchiyama, Yuri, Matsumoto, Naomichi, Nishimura, Kunihiro, Ohara, Osamu

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Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1‐RUNX1T1 transcripts... von Sasaki, Koji, Tsujimoto, Shinichi, Miyake, Mayuko, Uchiyama, Yuri, Ikeda, Junji, Yoshitomi, Masahiro, Shimosato, Yuko, Tokumasu, Mayu, Matsuo, Hidemasa, Yoshida, Kenichi, Ohki, Kentaro, Kaburagi, Taeko, Yamato, Genki, Hara, Yusuke, Takeuchi, Masanobu, Kinoshita, Akitoshi, Tomizawa, Daisuke, Taga, Takashi, Adachi, Souichi, Tawa, Akio, Horibe, Keizo, Hayashi, Yasuhide, Matsumoto, Naomichi, Ito, Shuichi, Shiba, Norio

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