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ENFERMEDAD DE VON HIPPEL-LINDAU Y EMBARAZO

La Enfermedad de Von Hippel-Lindau es un síndrome hereditario, autosómico dominante asociado a la mutación de un gen supresor tumoral localizado en cromosoma 3p25-26 que tiene riesgo genético esperado de desarrollar hemangioblastoma múltiple en cerebro, médula y retina, feocromocitoma, carcino...

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Bibliographic Details
Main Authors:	Jorge Hasbun H. (Author), Melchor Lemp M. (Author), Julio Nazer H. (Author)
Format:	Book
Published:	Permanyer, 2005-01-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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