Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
Moradkhani, Kamran, Cuisset, Laurence, Boisseau, Pierre, Pichon, Olivier, Lebrun, Marine, Hamdi‐Rozé, Houda, Maurin, Marie‐Laure, Gruchy, Nicolas, Manca‐Pellissier, Marie‐Christine, Malzac, Perrine, Bilan, Frédéric, Audrezet, Marie‐Pierre, Saugier‐Veber, Pascale, Fauret‐Amsellem, Anne‐Laure, Missirian, Chantal, Kuentz, Paul, Egea, Gregory, Guichet, Agnès, Creveaux, Isabelle, Janel, Caroline, Harzallah, Ines, Touraine, Renaud, Goumy, Carole, Joyé, Nicole, Puechberty, Jacques, Haquet, Emmanuelle, Chantot‐Bastaraud, Sandra, Schmitt, Sébastien, Gosset, Philippe, Duban‐Bedu, Bénédicte, Delobel, Bruno, Vago, Philippe, Vialard, François, Gomes, Denise Molina, Siffroi, Jean‐Pierre, Bonnefont, Jean‐Paul, Dupont, Jean‐Michel, Jonveaux, Philippe, Doco‐Fenzy, Martine, Sanlaville, Damien, Le Caignec, Cédric
Published in Prenatal diagnosis (01.10.2019)
Published in Prenatal diagnosis (01.10.2019)
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Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies
Kleinfinger, Pascale, Lohmann, Laurence, Luscan, Armelle, Trost, Detlef, Bidat, Laurent, Debarge, Véronique, Castaigne, Vanina, Senat, Marie-Victoire, Brechard, Marie-Pierre, Guilbaud, Lucie, Le Guyader, Gwenaël, Satre, Véronique, Laurichesse Delmas, Hélène, Lallaoui, Hakima, Manca-Pellissier, Marie-Christine, Boughalem, Aicha, Valduga, Mylene, Hodeib, Farah, Benachi, Alexandra, Costa, Jean Marc
Published in Journal of clinical medicine (01.08.2020)
Published in Journal of clinical medicine (01.08.2020)
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Antenatal prognostic factor of fetal echogenic bowel
Ronin, Candice, Mace, Pierre, Stenard, Fabien, Loundou, Anderson, Capelle, Marianne, Mortier, Isabelle, Pellissier, Marie Christine, Sigaudy, Sabine, Levy, Annie, D’ercole, Claude, Hoffmann, Pascale, Merrot, Thierry, Lopater, Jonathan, De Lagausie, Pascal, Philip, Nicole, Bretelle, Florence
Published in European Journal of Obstetrics & Gynecology and Reproductive Biology (01.05.2017)
Published in European Journal of Obstetrics & Gynecology and Reproductive Biology (01.05.2017)
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Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome
Bretelle, Florence, Beyer, Laura, Pellissier, Marie Christine, Missirian, Chantal, Sigaudy, Sabine, Gamerre, Marc, D’Ercole, Claude, Philip, Nicole
Published in European journal of medical genetics (01.11.2010)
Published in European journal of medical genetics (01.11.2010)
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Journal Article
Transmission of mental retardation with fragile X site by two normal transmitter brothers
Pellissier, M C, Voelckel, M A, Piquet, C, Mattei, M G, Mattei, J F
Published in American journal of medical genetics (01.02.1991)
Published in American journal of medical genetics (01.02.1991)
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Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndrome
Voelckel, M A, Pellissier, M C, Piquet, C, N'Guyen, C, Boccaccio, I, Philip, N, Mattei, J F
Published in American journal of medical genetics (01.02.1991)
Published in American journal of medical genetics (01.02.1991)
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