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Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation by Jun Mori, Tatsuji Hasegawa, Yosuke Miyamoto, Kazumasa Kitamura, Hidechika Morimoto, Takenori Tozawa, Ritsuko Kimata Pooh, Tomohiro Chiyonobu
Published 2022-06-01
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Successful treatment of a hepatic-hemangioendothelioma infant presenting with hypothyroidism and tetralogy of Fallot by Akari Takai, Tomoko Iehara, Mitsuru Miyachi, Yoshiki Okumura, Tatsuji Hasegawa, Sachiko Tokuda, Kazuyuki Ikeda, Masaaki Yamagishi, Tatsuro Tajiri, Hajime Hosoi
Published 2018-04-01
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Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects by Takanobu Inoue, Akie Nakamura, Tomoko Fuke, Kazuki Yamazawa, Shinichiro Sano, Keiko Matsubara, Seiji Mizuno, Yoshika Matsukura, Chie Harashima, Tatsuji Hasegawa, Hisakazu Nakajima, Kumi Tsumura, Zenro Kizaki, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami
Published 2017-05-01
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