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Tuesday, 07 January 2025

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Editor

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Assuming opitz-kaveggia is required, and syndrome is required, the following 2 results were found.

  1. Opitz-Kaveggia Syndrome (OKS)https://cnke.org/articles/361

    in the CASK gene (Xp11). FGS3: Mapped to Xp22.3. FGS5: Mapped to Xq22.3. MED12 gene mutation should be reserved for Opitz-Kaveggia syndrome. Clinical Features Initial descriptions included mental retardation, large head, imperforate anus, congenital...

    • Type: Article
    • Author: Editor
    • Category: Home

  2. Opitz-Kaveggia Syndrome (OKS)https://cnke.org/topics/opitz-kaveggia-syndrome-oks

    • Type: Tag
    • Author: Editor
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