Zusammenfassung
Das Happle-Syndrom ist ein X-chromosomal dominant vererbtes Leiden, welches nur im weiblichen Geschlecht auftritt [4, 5]. Deshalb hat man bislang angenommen, daß das Gen bei männlichen Embryonen stets letal wirkt, und diese betroffenen Jungen schon in utero absterben.
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Literatur
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© 1993 Springer-Verlag Berlin Heidelberg
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Traupe, H. (1993). Molekulare Analysen zum Happle-Syndrom: Mögliche Beteiligung einer unstabilen Prämutation. In: Braun-Falco, O., Plewig, G., Meurer, M. (eds) Fortschritte der praktischen Dermatologie und Venerologie. Fortschritte der praktischen Dermatologie und Venerologie, vol 13. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78163-6_51
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DOI: https://doi.org/10.1007/978-3-642-78163-6_51
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