Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11 (Q24676110)

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Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11
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    Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11 (English)
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    O Bartsch
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    W Wuyts
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    W Van Hul
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    J T Hecht
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    P Meinecke
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    D Hogue
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    W Werner
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    B Zabel
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    G K Hinkel
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    C M Powell
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    L G Shaffer
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    P J Willems
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    April 1996
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    58
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    734-42
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    4
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