Lloveras E - Search Results

1

Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience.

Cirigliano V, Voglino G, Ordoñez E, Marongiu A, Paz Cañadas M, Ejarque M, Rueda L, Lloveras E, Fuster C, Adinolfi M. Cirigliano V, et al. Among authors: lloveras e. Prenat Diagn. 2009 Jan;29(1):40-9. doi: 10.1002/pd.2192. Prenat Diagn. 2009. PMID: 19173345

2

Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications.

Cirigliano V, Voglino G, Marongiu A, Cañadas P, Ordoñez E, Lloveras E, Plaja A, Fuster C, Adinolfi M. Cirigliano V, et al. Among authors: lloveras e. Ann N Y Acad Sci. 2006 Sep;1075:288-98. doi: 10.1196/annals.1368.039. Ann N Y Acad Sci. 2006. PMID: 17108223

3

Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies.

Cirigliano V, Ejarque M, Cañadas MP, Lloveras E, Plaja A, Perez MM, Fuster C, Egozcue J. Cirigliano V, et al. Among authors: lloveras e. Mol Hum Reprod. 2001 Oct;7(10):1001-6. doi: 10.1093/molehr/7.10.1001. Mol Hum Reprod. 2001. PMID: 11574670 Clinical Trial.

4

Prenatal diagnosis of an interstitial 12q chromosome deletion.

Pérez Sánchez C, Ayensa F, Lloveras E, Zamora L, Cirigliano V, Pérez E, Plaja A. Pérez Sánchez C, et al. Among authors: lloveras e. Ann Genet. 2004 Apr-Jun;47(2):177-9. doi: 10.1016/j.anngen.2003.10.006. Ann Genet. 2004. PMID: 15183750

5

Supernumerary ring chromosome: an etiology for Pallister-Killian syndrome?

Lloveras E, Canellas A, Cirigliano V, Català V, Cerdan C, Plaja A. Lloveras E, et al. Fetal Diagn Ther. 2013;34(3):172-5. doi: 10.1159/000347049. Epub 2013 Mar 6. Fetal Diagn Ther. 2013. PMID: 23485930

6

Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region.

Barranco L, Costa M, Lloveras E, Ordóñez E, Maiz N, Hernando C, Villa O, Cirigliano V, Plaja A. Barranco L, et al. Among authors: lloveras e. Cytogenet Genome Res. 2015;147(4):209-11. doi: 10.1159/000444600. Epub 2016 Mar 15. Cytogenet Genome Res. 2015. PMID: 26974471

7

Ectopic nucleolus organizer regions in a patient with premature ovarian failure.

Lloveras E, Zamora L, Pérez C, Fuster C, Andreu S, Plaja A. Lloveras E, et al. Fertil Steril. 2006 Oct;86(4):1001.e15-6. doi: 10.1016/j.fertnstert.2006.02.125. Fertil Steril. 2006. PMID: 17027366 Free article.

8

Two cases of tetrasomy 9p syndrome with tissue limited mosaicism.

Lloveras E, Pérez C, Solé F, Zamora L, Lladonosa A, Espinet B, Silvestre E, Serra J, Vendrell T, Fernández B, Salido M, Plaja A. Lloveras E, et al. Am J Med Genet A. 2004 Feb 1;124A(4):402-6. doi: 10.1002/ajmg.a.20447. Am J Med Genet A. 2004. PMID: 14735590

9

A female infant with a 46,XX/48,XY, +8, +10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?

Lloveras E, Lecumberri JM, Pérez C, Melero C, Zamora L, Sánchez MA, Solé F, Plaja A. Lloveras E, et al. Prenat Diagn. 2001 Oct;21(10):896-7. doi: 10.1002/pd.174. Prenat Diagn. 2001. PMID: 11746139 No abstract available.

10

Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: a possible recurrent chromosome aberration.

Plaja A, Lloveras E, Martinez-Bouzas C, Barreña B, Del Campo M, Fernández A, Herrero M, Barranco L, Palau N, López-Aríztegui MA, Català V, Tejada MI. Plaja A, et al. Among authors: lloveras e. Am J Med Genet A. 2013 Sep;161A(9):2363-8. doi: 10.1002/ajmg.a.36102. Epub 2013 Jul 25. Am J Med Genet A. 2013. PMID: 23894094

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