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April 13, 2024

13
Apr

Deleción 1p36 (Monosomía 1p36)

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Síndrome de Deleción 1p36 Ocurriendo en 1 de cada 5,000 a 10,000 nacimientos vivos, la monosomía 1p36 es el síndrome de deleción subtelomérica más común en humanos1. Los primeros informes de individuos con monosomía parcial del cromosoma 1p36 se publicaron a principios de la década de 19802. Identificar pacientes con...
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