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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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16700088
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Colomer J, Gooding R, Angelicheva D, King RH, Guillén-Navarro E, Parman Y, Nascimento A, Conill J, Kalaydjieva L. Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2. Neuromuscul Disord. 2006 Jul;16(7):449-53. Epub 2006 Jun 27. PubMed PMID: 16806930.
AÑO: 2006; IF: 2.615
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López-Exposito I, Guillén-Navarro E, Bafallíu JA, Bernabé MC, Escalona A, Fuster C. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin. Eur J Med Genet. 2006 Nov-Dec;49(6):511-5. Epub 2006 Jun 23. PubMed PMID: 16824814.
AÑO: 2006; IF: 1.614
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Fernández-Barreiro A, Guillén-Navarro E, Tortosa-Conesa D, Meca-Lallana JE. [The current state of acute intermittent porphyria in the region of Murcia]. Rev Neurol. 2004 May 1-15;38(9):895-6. Spanish. PubMed PMID: 15152361.
AÑO: 2004; IF: 0.485
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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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