(Q31055913)
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Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation (English)
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M. J. Pettenati
N. Rao
C. Johnson
R. Hayworth
K. Crandall
O. Huff
1 August 1992
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602-606
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Identifiers
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