论文信息 - Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1 - 字舞流文

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

K. Tanaka | N. Wakamatsu | T. Yamanaka | T. Kuroda | T. Saji | Y. Yamada | K. Yamada | M. Nagaya | M. Segawa | Y. Nomura | M. Mimaki | T. Ezoe | N. Ishihara | K. Miura | T. Kumagai | T. Ohki | K. Hoshino | K. Ohya | H. Nitta | M. Yoneda | Y. Hara | J. Kato | N. Kuwabara | Y. Kobayashi | M. Matsushima | A. Onuma | M. Saeki | Yasukazu Yamada | Toshiyuki Kumagai | Masahiro Nagaya | Tsutomu Saji | Yoshiko Nomura | Naoko Ishihara | Keiko Tanaka | Takashi Ohki | Tatsuo Kuroda | Keiko Tanaka