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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. Onuma
Research output: Contribution to journal › Article › peer-review
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