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46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosis.
Rodriguez-Revenga L, Badenas C, Madrigal I, Sánchez A, Soler A, Carrió A, Milà M. Rodriguez-Revenga L, et al. Among authors: mila m. Prenat Diagn. 2005 Jun;25(6):448-50. doi: 10.1002/pd.1150. Prenat Diagn. 2005. PMID: 15966059
A retrospective and theoretical evaluation of rapid methods for detecting chromosome abnormalities and their implications on genetic counseling based on a series of 3868 CVS diagnoses.
Soler A, Morales C, Badenas C, Rodríguez-Revenga L, Carrió A, Margarit E, Costa D, Borrell A, Goncé A, Milà M, Sánchez A. Soler A, et al. Among authors: mila m. Fetal Diagn Ther. 2008;23(2):126-31. doi: 10.1159/000111592. Epub 2007 Nov 26. Fetal Diagn Ther. 2008. PMID: 18046070
Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes.
Morales C, Soler A, Badenas C, Rodríguez-Revenga L, Nadal A, Martínez JM, Mademont-Soler I, Borrell A, Milà M, Sánchez A. Morales C, et al. Among authors: mila m. Fertil Steril. 2009 Jul;92(1):393.e5-9. doi: 10.1016/j.fertnstert.2009.03.090. Epub 2009 May 13. Fertil Steril. 2009. PMID: 19442969 Free article.
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: mila m. 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.
Pilot study for the neonatal screening of fragile X syndrome.
Rifé M, Mallolas J, Badenas C, Tazón B, Miguélez MR, Pàmpols T, Sànchez A, Milà M. Rifé M, et al. Among authors: mila m. Prenat Diagn. 2002 Jun;22(6):459-62. doi: 10.1002/pd.346. Prenat Diagn. 2002. PMID: 12116303
191 results