檢索結果 - Maki Ogawa
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Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome 由 Masatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, Maki Ogawa, Fumihiko Suzuki, Takema Kato, Shunsuke Miyai, Rie Kawamura, Hidehito Inagaki, Hiroki Kurahashi, Jun Murotsuki
出版 2019索引號: 載入...Connect to this object online.
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