(Q48455961)
Statements
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A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum (English)
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Elke Holinski-Feder
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Udo Koehler
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Birgit Ertl-Wagner
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Juergen Kunz
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Arpad von Moers
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Hubertus von Voss
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Chayim Schell-Apacik
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8 September 2009
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169
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4
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463-468
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Identifiers
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