Effects of preterm birth on intrinsic fluctuations in neonatal cerebral activity examined using optical imaging.

par Yutaka Fuchino, Nozomi Naoi, Minoru Shibata, Fusako Niwa, Masahiko Kawai, Yukuo Konishi, Kazuo Okanoya, Masako Myowa-Yamakoshi
Publié 2013

TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.

par Tsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, Masahiko Kawai, Takeshi Nagashima, Ryo Funayama, Keiko Nakayama, Shinichi Nakashima, Fumiko Kato, Maki Fukami, Yoko Aoki, Yoichi Matsubara
Publié 2014