Mediano C - Search Results

1

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.

Armengol L, Nevado J, Serra-Juhé C, Plaja A, Mediano C, García-Santiago FA, García-Aragonés M, Villa O, Mansilla E, Preciado C, Fernández L, Ángeles Mori M, García-Pérez L, Lapunzina PD, Pérez-Jurado LA. Armengol L, et al. Among authors: mediano c. Hum Genet. 2012 Mar;131(3):513-23. doi: 10.1007/s00439-011-1095-5. Hum Genet. 2012. PMID: 21975797 Free PMC article. Clinical Trial.

2

Assessment of QF-PCR as the first approach in prenatal diagnosis.

Badenas C, Rodríguez-Revenga L, Morales C, Mediano C, Plaja A, Pérez-Iribarne MM, Soler A, Clusellas N, Borrell A, Sánchez MÁ, Miró E, Sánchez A, Milà M, Jiménez W. Badenas C, et al. Among authors: mediano c. J Mol Diagn. 2010 Nov;12(6):828-34. doi: 10.2353/jmoldx.2010.090224. Epub 2010 Oct 1. J Mol Diagn. 2010. PMID: 20889556 Free PMC article.

3

Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR.

Cirigliano V, Cañadas P, Plaja A, Ordoñez E, Mediano C, Sánchez A, Farrán I. Cirigliano V, et al. Among authors: mediano c. Prenat Diagn. 2003 Aug;23(8):629-33. doi: 10.1002/pd.655. Prenat Diagn. 2003. PMID: 12913868

4

Prenatal diagnosis of a rare chromosomal instability syndrome: variegated aneuploidy related to premature centromere division (PCD).

Plaja A, Mediano C, Cano L, Vendrell T, Sarret E, Farràn I, Sánchez MA. Plaja A, et al. Among authors: mediano c. Am J Med Genet A. 2003 Feb 15;117A(1):85-6. doi: 10.1002/ajmg.a.10810. Am J Med Genet A. 2003. PMID: 12548747 No abstract available.

5

Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis.

Rigola MA, Plaja A, Mediano C, Miró R, Egozcue J, Fuster C. Rigola MA, et al. Among authors: mediano c. Am J Med Genet. 2001 Nov 15;104(1):37-41. doi: 10.1002/ajmg.1584. Am J Med Genet. 2001. PMID: 11746025

6

Terminal deletion of Xp in a dysmorphic anencephalic fetus.

Plaja A, Vendrell T, Sarret E, Torán N, Mediano C. Plaja A, et al. Among authors: mediano c. Prenat Diagn. 1994 May;14(5):410-2. doi: 10.1002/pd.1970140512. Prenat Diagn. 1994. PMID: 8084861

7

Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.

Plaja A, Mediano C, Farran I, Vendrell T, Toran N, Gili T, Sanchez MA, Sarret E. Plaja A, et al. Among authors: mediano c. Ann Genet. 1998;41(1):52-5. Ann Genet. 1998. PMID: 9599652

8

Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.

Plaja A, Vendrell T, Smeets D, Sarret E, Gili T, Català V, Mediano C, Scheres JM. Plaja A, et al. Among authors: mediano c. Am J Med Genet. 2001 Jan 22;98(3):216-23. doi: 10.1002/1096-8628(20010122)98:3<216::aid-ajmg1091>3.0.co;2-0. Am J Med Genet. 2001. PMID: 11169558 Review.

9

Early amniocentesis with the filtration technique: neonatal outcome in 123 singleton pregnancies.

Farrán I, Sánchez MA, Mediano C, Plaja A, Guzmán A, de la Riva AM, Cabero L. Farrán I, et al. Among authors: mediano c. Prenat Diagn. 2002 Oct;22(10):859-63. doi: 10.1002/pd.424. Prenat Diagn. 2002. PMID: 12378565

10

Terminal deletion of 6p: report of a new case.

Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E. Plaja A, et al. Among authors: mediano c. Ann Genet. 1994;37(4):196-9. Ann Genet. 1994. PMID: 7710255

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