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Genetisch aktiv in Mesenchym-Zellen des Augenlides

FOXL2. 3q23. ...und im Ovar nach der Pubertät. Mutationen in FOXL2 Gen in 3q23 verursachen BPES I und POF Syndrom. Genetisch aktiv in Mesenchym-Zellen des Augenlides.

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Genetisch aktiv in Mesenchym-Zellen des Augenlides

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  1. FOXL2 3q23 ...und im Ovar nach der Pubertät Mutationen in FOXL2 Gen in 3q23 verursachen BPES I und POF Syndrom Genetisch aktiv in Mesenchym-Zellen des Augenlides Peter H. Vogt, Sektion Mol. Genetik & Fertilitätsstörungen, Gynäkol. Endokrinol. & Reproduktionsmedizin, Univ. Heidelberg

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