Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Sammuel E.V. Linsen"'
Autor:
Seiken Takayama, Daisuke Yamaguchi, Marius J. Giphart, Shunichi Shiozawa, Seiamak Bahram, Satoshi Makino, Jerzy K. Kulski, Kei Fujimoto, Yuu Nakami, Tomoki Ikuta, Gen Tamiya, Atsuo Taniguchi, Koh Furugaki, Minori Shinya, Takatoshi Minezaki, Yasuo Suzuki, Akira Oka, Yuuichi Hoshina, Joji Mochida, Takashi Gojobori, Koichi Okamoto, Wataru Yukawa, Yoko Yoshikawa, Satoshi Ando, Koichiro Komai, Manabu Yonekura, Tadashi Imanishi, Takuya Saruwatari, Minoru Kimura, Masaru Yagura, Hisashi Yamanaka, Shuhei Mano, Yasuyuki Nozaki, Takaho A. Endo, Tomomitsu Hotta, Suenori Chiku, Hidetoshi Inoko, Hideo Ishibashi, Naoyuki Kamatani, Toru Fukazawa, Ryo Nakashige, Hiroshi Hashimoto, Sammuel E.V. Linsen, Toshiko Matsumoto
Publikováno v:
Human molecular genetics. 14(16)
A major goal of current human genome-wide studies is to identify the genetic basis of complex disorders. However, the availability of an unbiased, reliable, cost efficient and comprehensive methodology to analyze the entire genome for complex disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a3336678c803d5d45dd76e0d6656b6f
https://pubmed.ncbi.nlm.nih.gov/16000323
https://pubmed.ncbi.nlm.nih.gov/16000323
