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 journalArticlepeer-review

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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