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C Hayakawa

Showing results (11-20 of 20) with videos related to

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Epilepsia|November 1, 1992
Epilepsy in Angelman syndrome associated with chromosome 15q deletionA Matsumoto, T Kumagai, K Miura, et al.
The Tohoku Journal of Experimental Medicine|November 1, 1987
Guanidino compounds in hyperargininemiaN Mizutani, C Hayakawa, Y Ohya, et al.
Biochemistry International|March 1, 1984
Selective binding behavior of zinc(II) and copper(II) ions to their native sites of apo-bovine superoxide dismutaseJ Hirose, M Yamada, C Hayakawa, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|December 1, 1987
[The development of a radioimmunoassay for somatostatin]T Kimura, S Ito, S Ishii, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|September 1, 1987
[The measurements of somatostatin by radioimmunoassay]H Hayashi, T Kimura, S Ishii, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|March 1, 1987
[Hepatitis B virus and epidemiological study on efficacy of HBIG for the prevention of type B hepatitis after accidental exposures among medical staff]T Kimura, M Higaki, M Shikone, et al.
European Journal of Pediatrics|September 1, 1991
Absence of erythrocyte arginase protein in Japanese patients with hyperargininemiaC Hayakawa, S Aono, H Keino, et al.
Journal of Intellectual Disability Research : JIDR|January 6, 2000
Difficulty in writing Japanese semantic characters in a 9-year-old boy with Williams syndromeM Nakamura, K Hara, T Watamaki, et al.
Human Mutation|August 29, 2001
Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlationY Yamada, K Miura, T Kumagai, et al.
American Journal of Human Genetics|October 10, 2001
Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical featuresK Yamada, Y Yamada, N Nomura, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Epilepsia|November 1, 1992
Epilepsy in Angelman syndrome associated with chromosome 15q deletionA Matsumoto, T Kumagai, K Miura, et al.
The Tohoku Journal of Experimental Medicine|November 1, 1987
Guanidino compounds in hyperargininemiaN Mizutani, C Hayakawa, Y Ohya, et al.
Biochemistry International|March 1, 1984
Selective binding behavior of zinc(II) and copper(II) ions to their native sites of apo-bovine superoxide dismutaseJ Hirose, M Yamada, C Hayakawa, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|December 1, 1987
[The development of a radioimmunoassay for somatostatin]T Kimura, S Ito, S Ishii, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|September 1, 1987
[The measurements of somatostatin by radioimmunoassay]H Hayashi, T Kimura, S Ishii, et al.
Kanagawa Shigaku. the Journal of the Kanagawa Odontological Society|March 1, 1987
[Hepatitis B virus and epidemiological study on efficacy of HBIG for the prevention of type B hepatitis after accidental exposures among medical staff]T Kimura, M Higaki, M Shikone, et al.
European Journal of Pediatrics|September 1, 1991
Absence of erythrocyte arginase protein in Japanese patients with hyperargininemiaC Hayakawa, S Aono, H Keino, et al.
Journal of Intellectual Disability Research : JIDR|January 6, 2000
Difficulty in writing Japanese semantic characters in a 9-year-old boy with Williams syndromeM Nakamura, K Hara, T Watamaki, et al.
Human Mutation|August 29, 2001
Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlationY Yamada, K Miura, T Kumagai, et al.
American Journal of Human Genetics|October 10, 2001
Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical featuresK Yamada, Y Yamada, N Nomura, et al.
Pageof 2