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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Martínez-Lage JF, Ruíz-Espejo AM, Gilabert A, Pérez-Espejo MA, Guillén-Navarro E. Positional skull deformities in children: skull deformation without synostosis. Childs Nerv Syst. 2006 Apr;22(4):368-74. Epub 2005 Oct 20. PubMed PMID: 16237569.
AÑO: 2006; IF: 1.257
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Guillén-Navarro E, Glóver-López G. [Monogenic causes of X-linked mental retardation]. Rev Neurol. 2006 Jan 7;42 Suppl 1:S45-9. Review. Spanish. PubMed PMID: 16506132.
AÑO: 2006; IF: 0.528
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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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López I, Bafalliu JA, Bernabé MC, García F, Costa M, Guillén-Navarro E. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects. Prenat Diagn. 2006 Jun;26(6):577-80. PubMed PMID: 16700088.
AÑO: 2006; IF: 1.514
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Pabellón Docente del Hospital
Clínico Universitario Virgen de la Arrixaca - 3ª Planta
C/ Campo 12, 30120 - El Palmar - Murcia, España
+34 968359767
+34 968381298