Exclusión prenatal del síndrome de von Hippel-Lindau en una familia mexicana con una mutación nueva en el gen VHL
2014; Mexican Association of Gynecology and Obstetrics; Volume: 82; Issue: 03 Linguagem: Inglês
ISSN
2594-2034
AutoresOscar F. Chacón‐Camacho, Jesús Benítez-Granados, Juan Carlos Zenteno,
Tópico(s)Medical Imaging and Pathology Studies
ResumoBackground: von Hippel-Lindau (VHL) disease is an autosomal dominant and familial multisystemic syndrome that is caused by the
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