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Hirobumi Sugawara

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American Journal of Medical Genetics. Part A|April 23, 2004
A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophyRumiko Kato, Jun Kawamura, Hirobumi Sugawara, et al.
Genomics|July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
American Journal of Medical Genetics|September 5, 2002
Duplication of 8p23.2: a benign cytogenetic variant?Naoki Harada, Jun Takano, Tatsuro Kondoh, et al.
Journal of Human Genetics|April 17, 2002
A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feetShinji Kondoh, Hirobumi Sugawara, Naoki Harada, et al.
American Journal of Human Genetics|April 11, 2003
Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndromeNoriko Miyake, Naohiro Kurotaki, Hirobumi Sugawara, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 23, 2004
A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophyRumiko Kato, Jun Kawamura, Hirobumi Sugawara, et al.
Genomics|July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
American Journal of Medical Genetics|September 5, 2002
Duplication of 8p23.2: a benign cytogenetic variant?Naoki Harada, Jun Takano, Tatsuro Kondoh, et al.
Journal of Human Genetics|April 17, 2002
A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feetShinji Kondoh, Hirobumi Sugawara, Naoki Harada, et al.
American Journal of Human Genetics|April 11, 2003
Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndromeNoriko Miyake, Naohiro Kurotaki, Hirobumi Sugawara, et al.
Pageof 1