Norio Niikawa - bibliography

Bibliography

• I. Hatada, Akira Nabetani, Hiroko Morisaki, Zhenghan Xin, Sachiko Ohishi, Hidefumi Tonoki, Norio Niikawa, Masahiro Inoue, Yosuke Komoto, Akira Okada, Elisabeth Steichen, Hirofumi Ohashi, Yoshimitsu Fukushima, Masahiro Nakayama, Tsunehiro Mukai:
  New p57KIP2 mutations in Beckwith-Wiedemann syndrome.
  Human Genetics, Berlin, 1976, 100 (5/6), 681-683
• Izuho Hatada, Johji Inazawa, Tatsuo Abe, Masahiro Nakayama, Yasuhiko Kaneko, Yoshihiro Jinno, Norio Niikawa, Hirofumi Ohashi, Yoshimitsu Fukushima, Kazuki Iida, Chikao Yutani, Shun-ichi Takahashi, Yoshihide Chiba, Sachiko Ohishi and Tsunehiro Mukai:
  Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.
  Human Molecular Genetics, Oxford, June 1996, 5 (6): 779.
• Takahiro Tsujita, Norio Niikawa, Hidejl Yamashita, Akira Imamura, Akira Hamada, Yoshibumi Nakane, and Yuji Okazaki:
  Genomic Discordance Between Monozygotic Twins Discordant for Schizophrenia.
  The American Journal of Psychiatry, Washington, 1997, 154 (11): 422.
  (Brief report).
• M. Fujimoto, Piranit Nik Kantaputra, Shiro Ikegawa, Yoshimitsu Fukushima, Shin-ichi Sonta, Masafumi Matsuo, Takafumi Ishida, Tadashi Matsumoto, Shinji Kondo, Hiroaki Tomita, Han-Xiang Deng, Michele D'urso, Maria Michela Rinaldi, Valerio Ventruto, Toshihisa Takagi, Yusuke Nakamura, Norio Niikawa:
  The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
  The Japanese Journal of Human Genetics. Jinrui Idengaku Zasshi, 1998, 43 (1): 32-36.
• Kiyonori Miura, Hideaki Masuzaki, Tadayuki Ishimaru, Norio Niikawa, Y. Jinno:
  Brief report - polymorphism report: A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5.
  The Japanese Journal of Human Genetics. Jinrui Idengaku Zasshi, 1998, 43 (4): 283-284.
• Kohzoh Mitsuya, Makiko Meguro, Maxwell P. Lee, Motonobu Katoh, Thomas C. Schulz, Hiroyuki Kugoh, Mitsuaki A. Yoshida, Norio Niikawa, Andrew P. Feinberg, Mitsuo Oshimura:
  LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.
  Human Molecular Genetics, Oxford, July 1998, 8 (7): 1209-1217.
• Kenji Maeda, Sachiko Matsuhashi, Katsuji Hori, Zhenghan Xin, Tsunehiro Mukai, Kazuo Tabuchi, Masayuki Egashira, Norio Niikawa:
  Cloning and Characterization of a Novel Human Gene, TM4SF6, Encoding a Protein Belonging to the Transmembrane 4 Superfamily, and Mapped to Xq22.
  Genomics, 1998, 52 (2): 240-242.