Diagnóstico molecular por reacción en cadena de la polimerasa del síndrome X frágil: aplicación de un protocolo diagnóstico en 50 familias del norte de España
Molecular diagnosis of fragile X syndrome by polymerase chain reaction: Application of a diagnostic protocol in 50 families from northern Spain
M. Durán Domíngueza,b, M. Molina Carrilloa, J. Fernández Toralc, T. Martínez Merinod, M.aA. López Arísteguie, A.I. Álvarez Retuertoa, M.aL. Onaindía Urquijoa, M.aI. Tejada Míngueza,
Corresponding author
itejada@hbas.osakidetza.net
Correspondencia: Unidad de Genética. Hospital de Basurto. Avda. Montevideo, 18. 48013Bilbao
Correspondencia: Unidad de Genética. Hospital de Basurto. Avda. Montevideo, 18. 48013Bilbao
a Unidad de Genética. Hospital de Basurto. Bilbao.
b Instituto de Biología y Genética Molecular. Facultad de Medicina. Universidad de Valladolid.
c Sección de Genética. Servicio de Pediatría. Hospital Central de Asturias.
d Laboratorio de Genética. Hospital de Cantabria. Santander.
e Laboratorio de Genética. Hospital de Cruces. Baracaldo. Bilbao.
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