江川 陽 | 株式会社日立製作所 社会イノベーション協創センタ
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概要
論文 | ランダム
- Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes
- Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation
- A Japanese trichothiodystrophy patient with XPD mutations
- Evidence for epistatic interactions in antiepileptic drug resistance
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population