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

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 ; Onuma, A ; Kuroda, T ; Yoneda, M ; Yamanaka, T ; Saeki, M ; Segawa, M ; Saji, T ; Nagaya, M ; Wakamatsu, N

Journal of medical genetics, 2004-05, Vol.41 (5), p.387-393 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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