Francisco Martínez
Unidad de Genética y Diagnóstico Prenatal
Hospital Universitario La Fe
Valencia
Spain
Name/email consistency: high
- Robust, easy, and dose-sensitive methylation test for the diagnosis of Prader-Willi and Angelman syndromes. Martínez, F., León, A.M., Monfort, S., Oltra, S., Roselló, M., Orellana, C. Genet. Test. (2006)
- Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family. Martínez, F., Martínez-Garay, I., Oltra, S., Moltó, M.D., Orellana, C., Monfort, S., Prieto, F., Tejada, I. Am. J. Med. Genet. A (2004)









