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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Francisco Martínez

Unidad de Genética y Diagnóstico Prenatal

Hospital Universitario La Fe

Valencia

Spain

[email]@gva.es

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Unidad de Genética y Diagnóstico Prenatal, Hospital Universitario La Fe, Valencia, Spain. 2006
  • Unidad de Genética, Hospital La Fe, Valencia, Spain. 2004

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
 
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