Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1

N. Ishihara, K. Yamada, Y. Yamada, K. Miura, J. Kato, N. Kuwabara, Y. Hara, Y. Kobayashi, K. Hoshino, Y. Nomura, M. Mimaki, K. Ohya, M. Matsushima, H. Nitta, K. Tanaka, M. Segawa, T. Ohki, T. Ezoe, T. Kumagai, A. OnumaT. Kuroda, M. Yoneda, T. Yamanaka, M. Saeki, M. Segawa, T. Saji, M. Nagaya, N. Wakamatsu

Research output: Contribution to journalArticle

56 Citations (Scopus)
Original languageEnglish
Pages (from-to)387-393
Number of pages7
JournalJournal of medical genetics
Volume41
Issue number5
DOIs
Publication statusPublished - 2004 May

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Ishihara, N., Yamada, K., Yamada, Y., Miura, K., Kato, J., Kuwabara, N., Hara, Y., Kobayashi, Y., Hoshino, K., Nomura, Y., Mimaki, M., Ohya, K., Matsushima, M., Nitta, H., Tanaka, K., Segawa, M., Ohki, T., Ezoe, T., Kumagai, T., ... Wakamatsu, N. (2004). Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1. Journal of medical genetics, 41(5), 387-393. https://doi.org/10.1136/jmg.2003.016154