Microwave assisted magnetic Recording: Physics and application to hard disk drives
Takagishi, Masayuki, Narita, Naoyuki, Nakagawa, Yuji, Nagasawa, Tazumi, Osamura, Ryo, Maeda, Tomoyuki, Yamada, Kenichiro
Published in Journal of magnetism and magnetic materials (01.12.2022)
Published in Journal of magnetism and magnetic materials (01.12.2022)
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Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome
Kondo, Yoko, Mizuno, Seiji, Ohara, Kei, Nakamura, Takeshi, Yamada, Kenichiro, Yamamori, Shunji, Hayakawa, Chiemi, Ishii, Takashi, Yamada, Yasukazu, Wakamatsu, Nobuaki
Published in American journal of medical genetics. Part A (01.02.2006)
Published in American journal of medical genetics. Part A (01.02.2006)
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Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation
Mizuno, Seiji, Yamada, Yasukazu, Yamada, Kenichiro, Nomura, Noriko, Wakamatsu, Nobuaki
Published in Congenital anomalies (01.06.2005)
Published in Congenital anomalies (01.06.2005)
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Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion
Yamada, Kenichiro, Aiba, Kaori, Kitaura, Yasuyuki, Kondo, Yusuke, Nomura, Noriko, Nakamura, Yuji, Fukushi, Daisuke, Murayama, Kei, Shimomura, Yoshiharu, Pitt, James, Yamaguchi, Seiji, Yokochi, Kenji, Wakamatsu, Nobuaki
Published in Journal of medical genetics (01.10.2015)
Published in Journal of medical genetics (01.10.2015)
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Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivation
Katoh, Kimiko, Aiba, Kaori, Fukushi, Daisuke, Yoshimura, Jun, Suzuki, Yasuyo, Mitsui, Jun, Morishita, Shinichi, Tuji, Shoji, Yamada, Kenichiro, Wakamatsu, Nobuaki
Published in Human mutation (01.08.2020)
Published in Human mutation (01.08.2020)
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