(Q40750796)
Statements
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A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p. (English)
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Uehara S
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Akai Y
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Takeyama Y
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Okamura K
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Takabayashi T
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Yajima A
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Natsui M
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Nakai H
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1 January 1993
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43
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1
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28-33
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Identifiers
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