Genética Médica

Los alelos intermedios del X frágiles: ¿afectan al riesgo reproductivo?

Please note: this is an automatic translation. To read the original version, please refer to the English or Italian page. Resumen El síndrome de X frágil es un trastorno hereditario causado por una expansión de repetición CGG en el gen FMR1. El síndrome se caracteriza por retraso mental leve a severo, que puede estar asociado

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