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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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16506132
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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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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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