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Diagnóstico prenatal de síndrome de Apert por mutación de novo en gen FGFR2
Prenatal diagnosis of Apert syndrome caused by de novo mutation in FGFR2 gene
G. Pia, A. Zúñigab,
Corresponding author
azuniga@hospital-ribera.com

Autor para correspondencia.
, J. Cerverac, M. Ortiza
a Servicio de Pediatría, Hospital Universitario de la Ribera, Alzira, Valencia, España
b Servicio de Genética y Biología Molecular, Hospital Universitario de la Ribera, Alzira, Valencia, España
c Servicio de Ginecología, Hospital Universitario de la Ribera, Alzira, Valencia, España
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ISSN: 16954033
Original language: Spanish
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