Gonzalez-Gonzalez MC - Search Results

1

Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family.

Trujillo MJ, Garcia-Sandoval B, Lorda-Sanchez I, Gimenez A, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, Ibañez A, Ramos C, Ayuso C. Trujillo MJ, et al. Among authors: gonzalez gonzalez mc. Ophthalmic Genet. 2000 Dec;21(4):251-6. Ophthalmic Genet. 2000. PMID: 11135497

2

Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.

Lorda-Sanchez I, Lopez-Pajares I, Roche MC, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, Ibañez A, Ramos C, Ayuso C. Lorda-Sanchez I, et al. Among authors: gonzalez gonzalez mc. Am J Med Genet. 2000 Dec 11;95(4):336-8. Am J Med Genet. 2000. PMID: 11186887

3

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

4

Early Huntington disease prenatal diagnosis by maternal semiquantitative fluorescent-PCR.

González-González MC, Trujillo MJ, Rodríguez de Alba M, Ramos C. González-González MC, et al. Neurology. 2003 Apr 8;60(7):1214-5. doi: 10.1212/01.wnl.0000056084.13096.8a. Neurology. 2003. PMID: 12682342 No abstract available.

5

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

6

Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparations.

Sanz R, Lorda-Sanchez I, Fernández-Moya JM, Cifuentes-Sulzberger S, Rodríguez de Alba M, Gonzalez-Gonzalez MC, Ibañez MA, Robledo M, Ayuso C, Ramos C. Sanz R, et al. Among authors: gonzalez gonzalez mc. Fetal Diagn Ther. 2001 Mar-Apr;16(2):95-7. doi: 10.1159/000053888. Fetal Diagn Ther. 2001. PMID: 11173955

7

Improvement in strategies for the non-invasive prenatal diagnosis of Huntington disease.

González-González MC, Garcia-Hoyos M, Trujillo-Tiebas MJ, Bustamante Aragonés A, Rodriguez de Alba M, Diego Alvarez D, Diaz-Recasens J, Ayuso C, Ramos C. González-González MC, et al. J Assist Reprod Genet. 2008 Sep-Oct;25(9-10):477-81. doi: 10.1007/s10815-008-9256-8. Epub 2008 Oct 14. J Assist Reprod Genet. 2008. PMID: 18853247 Free PMC article.

8

Prenatal diagnosis on fetal cells from maternal peripheral blood in cases of confined placental mosaicism.

Rodríguez de Alba M, González-González MC, Palomino P, Ramos C. Rodríguez de Alba M, et al. Prenat Diagn. 2000 Mar;20(3):264-5. Prenat Diagn. 2000. PMID: 10719336 No abstract available.

9

Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females.

Arce-Gonzalez R, Chacon-Camacho OF, Navas-Perez A, Gonzalez-Gonzalez MC, Martinez-Aguilar A, Zenteno JC. Arce-Gonzalez R, et al. Among authors: gonzalez gonzalez mc. Ophthalmic Genet. 2022 Apr;43(2):224-229. doi: 10.1080/13816810.2021.2002917. Epub 2021 Nov 29. Ophthalmic Genet. 2022. PMID: 34844512

10

Clinical and echographic long-term follow-up of a retinal macrocyst: a case report.

Serna-Ojeda JC, Pinkus-Herrera CD, Moreno-Londono MV, Rodriguez-Loaiza JL, Gonzalez-Gonzalez MC. Serna-Ojeda JC, et al. Among authors: gonzalez gonzalez mc. Case Rep Ophthalmol. 2014 Jun 5;5(2):168-71. doi: 10.1159/000363759. eCollection 2014 May. Case Rep Ophthalmol. 2014. PMID: 25028580 Free PMC article.

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