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M Segawa

Showing results (191-200 of 196) with videos related to

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The Japanese Journal of Antibiotics|May 1, 1982
[Clinical evaluation of cefotiam in internal medicine]S Kawamura, Y Sakata, Y Chiba, et al.
Journal of Gastroenterology|June 5, 2001
HBV-related fulminant hepatic failure: successful intensive medical therapy in a candidate for liver transplantationM Masuhara, T Yagawa, M Aoyagi, et al.
American Journal of Medical Genetics|September 20, 1996
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph diseaseK Endo, H Sasaki, A Wakisaka, et al.
Nature|August 5, 1998
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophyK Kobayashi, Y Nakahori, M Miyake, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, 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.
Pageof 20

Showing results (191-200 of 196) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 196 results.
The Japanese Journal of Antibiotics|May 1, 1982
[Clinical evaluation of cefotiam in internal medicine]S Kawamura, Y Sakata, Y Chiba, et al.
Journal of Gastroenterology|June 5, 2001
HBV-related fulminant hepatic failure: successful intensive medical therapy in a candidate for liver transplantationM Masuhara, T Yagawa, M Aoyagi, et al.
American Journal of Medical Genetics|September 20, 1996
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph diseaseK Endo, H Sasaki, A Wakisaka, et al.
Nature|August 5, 1998
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophyK Kobayashi, Y Nakahori, M Miyake, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, 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.
Pageof 20