[Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation]. / Exclusión prenatal del síndrome de von Hippel-Lindau en una familia Mexicana con una mutación nueva en el gen VHL.
Ginecol Obstet Mex
; 82(3): 163-9, 2014 Mar.
Article
in Es
| MEDLINE
| ID: mdl-24779271
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prenatal Diagnosis
/
Von Hippel-Lindau Tumor Suppressor Protein
/
Von Hippel-Lindau Disease
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Pregnancy
Country/Region as subject:
Mexico
Language:
Es
Journal:
Ginecol Obstet Mex
Year:
2014
Document type:
Article