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Glóver-López G, Guillén-Navarro E. [Fragile X syndrome]. Rev Neurol. 2006 Jan 7;42 Suppl 1:S51-4. Review. Spanish. PubMed PMID: 16506133.
AÑO: 2006; IF: 0.528
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16506133
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Carbonell P, Glover G, Fernández JA, Ramírez M, Marín C, Castellanos G, Parrilla P. [Hereditary pancreatitis caused by a new mutation in the trypsinogen gene. Report of a family]. Cir Esp. 2006 Apr;79(4):252-4. Spanish. PubMed PMID: 16753108.
AÑO: 2006
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Guillén-Navarro E, Carbonell P, Glover G, Sánchez-Solís M, Fernández-Barreiro A. Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria. Ann Hum Genet. 2004 Sep;68(Pt 5):509-14. PubMed PMID: 15469427.
AÑO: 2004; IF: 1.319
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