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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1976 1
1977 3
1978 1
1979 4
1981 2
1982 2
1985 2
1987 1
1989 2
1990 2
1991 1
1993 1
1994 1
1998 2
1999 3
2000 1
2001 1
2003 2
2004 2
2005 4
2006 3
2008 1
2024 0

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43 results

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Page 1
Tetraploidy in a liveborn infant.
López Pajares I, Delicado A, Diaz de Bustamante A, Pellicer A, Pinel I, Pardo M, Martin M. López Pajares I, et al. J Med Genet. 1990 Dec;27(12):782-3. doi: 10.1136/jmg.27.12.782. J Med Genet. 1990. PMID: 2074564 Free PMC article. Review.
Partial trisomy 14q.
Lopez Pajares I, Delicado A, Cobos PV, Lledo G, Peralta A. Lopez Pajares I, et al. Hum Genet. 1979 Jan 25;46(2):243-7. doi: 10.1007/BF00291928. Hum Genet. 1979. PMID: 422208
Craniofacial dyssynostosis: description of the first four Spanish cases and review.
Bermejo E, Félix V, Lapunzina P, Galán E, Soler V, Delicado A, Pantoja A, Márquez MD, García M, Mora E, Cuevas L, Ureta A, López-Pajares I, Martínez-Frías ML. Bermejo E, et al. Among authors: lopez pajares i. Am J Med Genet A. 2005 Jan 1;132A(1):41-8. doi: 10.1002/ajmg.a.30380. Am J Med Genet A. 2005. PMID: 15551327 Review.
Partial trisomy 20.
Delicado A, Lopez Pajares I, Vicente P, Gracia R. Delicado A, et al. Among authors: lopez pajares i. Ann Genet. 1981;24(1):54-6. Ann Genet. 1981. PMID: 6971621
Fragile X syndrome with extra microchromosome.
López-Pajares I, Delicado A, Pascual-Castroviejo I, López-Martin V, Moreno F, Garcia-Marcos JA. López-Pajares I, et al. Clin Genet. 1994 Apr;45(4):186-9. doi: 10.1111/j.1399-0004.1994.tb04020.x. Clin Genet. 1994. PMID: 8062436
Euchromatic variant 16p+. Implications in prenatal diagnosis.
López Pajares I, Villa O, Salido M, Mori MA, Gonzalez A, Lapunzina P, De Torres ML, Vallcorba I, Palomares M, Fernández L, Delicado A. López Pajares I, et al. Prenat Diagn. 2006 Jun;26(6):535-8. doi: 10.1002/pd.1454. Prenat Diagn. 2006. PMID: 16634122
Direct tandem duplication in chromosome 19q characterized by array CGH.
Palomares Bralo M, Delicado A, Lapunzina P, Velázquez Fragua R, Villa O, Angeles Mori M, Luisa de Torres M, Fernández L, Pérez Jurado LA, López Pajares I. Palomares Bralo M, et al. Among authors: lopez pajares i. Eur J Med Genet. 2008 May-Jun;51(3):257-63. doi: 10.1016/j.ejmg.2008.01.003. Epub 2008 Feb 2. Eur J Med Genet. 2008. PMID: 18342596
An excess of chromosome 1 breakpoints in male infertility.
Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N. Bache I, et al. Among authors: lopez pajares i. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911
[Partial trisomy 18q].
Darnaude MT, López Pajares I, Delicado A, García Frias E. Darnaude MT, et al. Among authors: lopez pajares i. An Esp Pediatr. 1987 Jun;26(6):460-2. An Esp Pediatr. 1987. PMID: 3631780 Spanish.
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al. Karadima G, et al. Among authors: lopez pajares i. Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8. doi: 10.1038/sj.ejhg.5200212. Eur J Hum Genet. 1998. PMID: 9801867
43 results