García-Hoyos M - Search Results

1

Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma.

González-González MC, García-Hoyos M, Trujillo MJ, Rodríguez de Alba M, Lorda-Sánchez I, Díaz-Recasens J, Gallardo E, Ayuso C, Ramos C. González-González MC, et al. Prenat Diagn. 2002 Oct;22(10):946-8. doi: 10.1002/pd.439. Prenat Diagn. 2002. PMID: 12378583

2

Huntington disease-unaffected fetus diagnosed from maternal plasma using QF-PCR.

González-González MC, Trujillo MJ, Rodríguez de Alba M, García-Hoyos M, Lorda-Sánchez I, Díaz-Recasens J, Ayuso C, Ramos C. González-González MC, et al. Prenat Diagn. 2003 Mar;23(3):232-4. doi: 10.1002/pd.570. Prenat Diagn. 2003. PMID: 12627425

3

Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa.

Bernal S, Calaf M, Garcia-Hoyos M, Garcia-Sandoval B, Rosell J, Adan A, Ayuso C, Baiget M. Bernal S, et al. J Med Genet. 2003 Jul;40(7):e89. doi: 10.1136/jmg.40.7.e89. J Med Genet. 2003. PMID: 12843338 Free PMC article. No abstract available.

4

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

5

Evaluation of SFRP1 as a candidate for human retinal dystrophies.

Garcia-Hoyos M, Cantalapiedra D, Arroyo C, Esteve P, Rodríguez J, Riveiro R, Trujillo MJ, Ramos C, Bovolenta P, Ayuso C. Garcia-Hoyos M, et al. Mol Vis. 2004 Jun 28;10:426-31. Mol Vis. 2004. PMID: 15235574 Free article.

6

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

7

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

8

Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.

Riveiro-Alvarez R, Trujillo-Tiebas MJ, Gimenez-Pardo A, Garcia-Hoyos M, Cantalapiedra D, Lorda-Sanchez I, Rodriguez de Alba M, Ramos C, Ayuso C. Riveiro-Alvarez R, et al. Mol Vis. 2005 Sep 2;11:705-12. Mol Vis. 2005. PMID: 16163268 Free article.

9

New approach for the refinement of the location of the X-chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocation.

García-Hoyos M, Sanz R, Diego-Alvarez D, Lorda-Sánchez I, Trujillo-Tiebas MJ, Cantalapiedra D, Ramos C, Ayuso C. García-Hoyos M, et al. Am J Med Genet A. 2005 Nov 1;138(4):365-8. doi: 10.1002/ajmg.a.30987. Am J Med Genet A. 2005. PMID: 16222660

10

Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.

Diego-Alvarez D, Ramos-Corrales C, Garcia-Hoyos M, Bustamante-Aragones A, Cantalapiedra D, Diaz-Recasens J, Vallespin-Garcia E, Ayuso C, Lorda-Sanchez I. Diego-Alvarez D, et al. Hum Reprod. 2006 Apr;21(4):958-66. doi: 10.1093/humrep/dei406. Epub 2005 Dec 16. Hum Reprod. 2006. PMID: 16361293

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

55 results

Search Page

Filters