González-González C - Search Results

1

Prenatal diagnosis on fetal cells from maternal blood: practical comparative evaluation of the first and second trimesters.

Rodríguez de Alba M, Palomino P, González-González C, Lorda-Sanchez I, Ibañez MA, Sanz R, Fernández-Moya JM, Ayuso C, Díaz-Recasens J, Ramos C. Rodríguez de Alba M, et al. Prenat Diagn. 2001 Mar;21(3):165-70. doi: 10.1002/1097-0223(200103)21:3<165::aid-pd29>3.0.co;2-f. Prenat Diagn. 2001. PMID: 11260601

2

Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.

Lorda-Sanchez I, Sanz R, Diaz-Guillen MA, Fernandez-Toral J, Heine-Suñer D, Rodriguez De Alba M, Gonzalez-Gonzalez C, Trujillo MJ, Ramos C, Rodriguez De Cordoba S, Ayuso C. Lorda-Sanchez I, et al. Genet Couns. 2002;13(2):171-7. Genet Couns. 2002. PMID: 12150218

3

Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism.

Lorda-Sanchez I, Trujillo MJ, Gomez-Garre P, de Alba MR, Gonzalez-Gonzalez C, García-Hoyos M, Ayuso C, Ramos C. Lorda-Sanchez I, et al. Am J Med Genet A. 2003 Aug 15;121A(1):20-4. doi: 10.1002/ajmg.a.10197. Am J Med Genet A. 2003. PMID: 12900896

4

Application of fetal DNA detection in maternal plasma: a prenatal diagnosis unit experience.

González-González C, Garcia-Hoyos M, Trujillo-Tiebas MJ, Lorda-Sanchez I, de Alba MR, Infantes F, Gallego J, Diaz-Recasens J, Ayuso C, Ramos C. González-González C, et al. J Histochem Cytochem. 2005 Mar;53(3):307-14. doi: 10.1369/jhc.4A6400.2005. J Histochem Cytochem. 2005. PMID: 15750008

5

Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages.

Diego-Alvarez D, Garcia-Hoyos M, Trujillo MJ, Gonzalez-Gonzalez C, Rodriguez de Alba M, Ayuso C, Ramos-Corrales C, Lorda-Sanchez I. Diego-Alvarez D, et al. Hum Reprod. 2005 May;20(5):1235-43. doi: 10.1093/humrep/deh781. Epub 2005 Mar 10. Hum Reprod. 2005. PMID: 15760965

6

Prenatal diagnosis of 46, XX male fetus.

Trujillo-Tiebas MJ, González-González C, Lorda-Sánchez I, Querejeta ME, Ayuso C, Ramos C. Trujillo-Tiebas MJ, et al. J Assist Reprod Genet. 2006 May;23(5):253-4. doi: 10.1007/s10815-005-9020-2. Epub 2006 May 25. J Assist Reprod Genet. 2006. PMID: 16724267 Free PMC article.

7

Detection of a paternally inherited fetal mutation in maternal plasma by the use of automated sequencing.

Bustamante-Aragones A, Garcia-Hoyos M, Rodriguez DE Alba M, Gonzalez-Gonzalez C, Lorda-Sanchez I, Diego-Alvarez D, Trujillo-Tiebas MJ, Ayuso C, Ramos C. Bustamante-Aragones A, et al. Ann N Y Acad Sci. 2006 Sep;1075:108-17. doi: 10.1196/annals.1368.014. Ann N Y Acad Sci. 2006. PMID: 17108199

8

Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers.

Bustamante-Aragones A, Rodriguez de Alba M, Gonzalez-Gonzalez C, Trujillo-Tiebas MJ, Diego-Alvarez D, Vallespin E, Plaza J, Ayuso C, Ramos C. Bustamante-Aragones A, et al. Haemophilia. 2008 May;14(3):593-8. doi: 10.1111/j.1365-2516.2008.01670.x. Epub 2008 Mar 4. Haemophilia. 2008. PMID: 18328062

9

New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma.

Bustamante-Aragones A, Gallego-Merlo J, Trujillo-Tiebas MJ, de Alba MR, Gonzalez-Gonzalez C, Glover G, Diego-Alvarez D, Ayuso C, Ramos C. Bustamante-Aragones A, et al. J Cyst Fibros. 2008 Nov;7(6):505-10. doi: 10.1016/j.jcf.2008.05.006. Epub 2008 Jun 24. J Cyst Fibros. 2008. PMID: 18573697 Free article. Clinical Trial.

10

Early noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosis.

Bustamante-Aragones A, Vallespin E, Rodriguez de Alba M, Trujillo-Tiebas MJ, Gonzalez-Gonzalez C, Diego-Alvarez D, Riveiro-Alvarez R, Lorda-Sanchez I, Ayuso C, Ramos C. Bustamante-Aragones A, et al. Mol Vis. 2008 Aug 4;14:1388-94. Mol Vis. 2008. PMID: 18682814 Free PMC article.

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