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Page 1
[Monozygotic heterocaryotic twins: prenatal diagnosis and management].
Barré M, Le Caignec C, Rival JM, Le Vaillant C, Salomon LJ, Boscher C, Philippe HJ, Ville Y, Vialard F, Winer N. Barré M, et al. Among authors: vialard f. Presse Med. 2009 Jul-Aug;38(7-8):1170-3. doi: 10.1016/j.lpm.2008.12.032. Epub 2009 Apr 17. Presse Med. 2009. PMID: 19375887 French. No abstract available.
Fetal gender: antenatal discrepancy between phenotype and genotype.
Bretelle F, Salomon L, Senat MV, Vialard F, Albert M, Roume J, Ville Y. Bretelle F, et al. Among authors: vialard f. Ultrasound Obstet Gynecol. 2002 Sep;20(3):286-9. doi: 10.1046/j.1469-0705.2002.00778.x. Ultrasound Obstet Gynecol. 2002. PMID: 12230454 Free article.
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.
Alberti A, Salomon LJ, Le Lorc'h M, Couloux A, Bussières L, Goupil S, Malan V, Pelletier E, Hyon C, Vialard F, Rozenberg P, Bouhanna P, Oury JF, Schmitz T, Romana S, Weissenbach J, Vekemans M, Ville Y. Alberti A, et al. Among authors: vialard f. Prenat Diagn. 2015 May;35(5):471-6. doi: 10.1002/pd.4561. Prenat Diagn. 2015. PMID: 25643828
A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH.
Poirsier C, Besseau-Ayasse J, Schluth-Bolard C, Toutain J, Missirian C, Le Caignec C, Bazin A, de Blois MC, Kuentz P, Catty M, Choiset A, Plessis G, Basinko A, Letard P, Flori E, Jimenez M, Valduga M, Landais E, Lallaoui H, Cartault F, Lespinasse J, Martin-Coignard D, Callier P, Pebrel-Richard C, Portnoi MF, Busa T, Receveur A, Amblard F, Yardin C, Harbuz R, Prieur F, Le Meur N, Pipiras E, Kleinfinger P, Vialard F, Doco-Fenzy M. Poirsier C, et al. Among authors: vialard f. Eur J Hum Genet. 2016 Jun;24(6):844-51. doi: 10.1038/ejhg.2015.219. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508576 Free PMC article.
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
Egloff M, Hervé B, Quibel T, Jaillard S, Le Bouar G, Uguen K, Saliou AH, Valduga M, Perdriolle E, Coutton C, Coston AL, Coussement A, Anselem O, Missirian C, Bretelle F, Prieur F, Fanget C, Muti C, Jacquemot MC, Beneteau C, Le Vaillant C, Vekemans M, Salomon LJ, Vialard F, Malan V. Egloff M, et al. Among authors: vialard f. Ultrasound Obstet Gynecol. 2018 Dec;52(6):715-721. doi: 10.1002/uog.18928. Ultrasound Obstet Gynecol. 2018. PMID: 29027723 Free article.
Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Hureaux M, Guterman S, Hervé B, Till M, Jaillard S, Redon S, Valduga M, Coutton C, Missirian C, Prieur F, Simon-Bouy B, Beneteau C, Kuentz P, Rooryck C, Gruchy N, Marle N, Plutino M, Tosca L, Dupont C, Puechberty J, Schluth-Bolard C, Salomon L, Sanlaville D, Malan V, Vialard F. Hureaux M, et al. Among authors: vialard f. Prenat Diagn. 2019 May;39(6):464-470. doi: 10.1002/pd.5449. Epub 2019 Apr 29. Prenat Diagn. 2019. PMID: 30896039
208 results