(Q43073711)
Statements
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Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1. (English)
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Ishihara N
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Yamada K
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Yamada Y
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Miura K
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Kato J
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Kuwabara N
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Hara Y
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Kobayashi Y
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Hoshino K
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Nomura Y
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Mimaki M
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Ohya K
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Matsushima M
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Nitta H
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Tanaka K
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Segawa M
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Ohki T
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Ezoe T
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Kumagai T
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Onuma A
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Kuroda T
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Yoneda M
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Yamanaka T
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Saeki M
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Segawa M
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Saji T
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Nagaya M
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Wakamatsu N
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1 May 2004
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41
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387-393
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Identifiers
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