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S Tsuji

Showing results (971-980 of 990) with videos related to

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Annals of Neurology|July 14, 2000
Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15Y Shibasaki, H Tanaka, K Iwabuchi, et al.
American Journal of Human Genetics|March 1, 1997
Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27H Matsumine, M Saito, S Shimoda-Matsubayashi, et al.
Clinical Genetics|March 1, 2017
Clinical and mutational spectrum of Japanese patients with Charcot-Marie-Tooth disease caused by GDAP1 variantsA Yoshimura, J-H Yuan, A Hashiguchi, et al.
Gene Therapy|November 19, 2010
Refined human artificial chromosome vectors for gene therapy and animal transgenesisY Kazuki, H Hoshiya, M Takiguchi, et al.
Annals of the New York Academy of Sciences|January 1, 1976
A cooperative study of sarcoidosis in Asia and Africa: descriptive epidemiologyY Hosoda, T Kosuda, M Yamamoto, et al.
Journal of Internal Medicine|July 22, 2020
IL-15 is a biomarker involved in the development of rapidly progressive interstitial lung disease complicated with polymyositis/dermatomyositisT Shimizu, T Koga, K Furukawa, et al.
Neurology|September 15, 2004
Beta-synuclein gene alterations in dementia with Lewy bodiesH Ohtake, P Limprasert, Y Fan, et al.
American Journal of Human Genetics|December 1, 1999
Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1H a Tomita, S Nagamitsu, K Wakui, et al.
Nature Genetics|November 1, 1996
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTK Sanpei, H Takano, S Igarashi, et al.
Journal of Human Genetics|November 28, 2001
Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)T Asaka, K Ikeuchi, S Okino, et al.
Pageof 99

Showing results (971-980 of 990) with videos related to

Sort By:
Pageof 99
Annals of Neurology|July 14, 2000
Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15Y Shibasaki, H Tanaka, K Iwabuchi, et al.
American Journal of Human Genetics|March 1, 1997
Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27H Matsumine, M Saito, S Shimoda-Matsubayashi, et al.
Clinical Genetics|March 1, 2017
Clinical and mutational spectrum of Japanese patients with Charcot-Marie-Tooth disease caused by GDAP1 variantsA Yoshimura, J-H Yuan, A Hashiguchi, et al.
Gene Therapy|November 19, 2010
Refined human artificial chromosome vectors for gene therapy and animal transgenesisY Kazuki, H Hoshiya, M Takiguchi, et al.
Annals of the New York Academy of Sciences|January 1, 1976
A cooperative study of sarcoidosis in Asia and Africa: descriptive epidemiologyY Hosoda, T Kosuda, M Yamamoto, et al.
Journal of Internal Medicine|July 22, 2020
IL-15 is a biomarker involved in the development of rapidly progressive interstitial lung disease complicated with polymyositis/dermatomyositisT Shimizu, T Koga, K Furukawa, et al.
Neurology|September 15, 2004
Beta-synuclein gene alterations in dementia with Lewy bodiesH Ohtake, P Limprasert, Y Fan, et al.
American Journal of Human Genetics|December 1, 1999
Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1H a Tomita, S Nagamitsu, K Wakui, et al.
Nature Genetics|November 1, 1996
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTK Sanpei, H Takano, S Igarashi, et al.
Journal of Human Genetics|November 28, 2001
Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy)T Asaka, K Ikeuchi, S Okino, et al.
Pageof 99