Treffer 1 - 11 von 11 für Suche 'Aubertin, Jonathan D', Suchdauer: 0,65s Treffer weiter einschränken
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    Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines von Dreux, Sophie, Rosenblatt, Jonathan, Benachi, Alexandra, Voirin‐Mathieu, Etienne, Muller, Françoise, Boitte, F., Denis, M. C., Lorenter, P., Jouval, M., Sitruk, B., Suybeng, V., Herbreteau, S., Treyssac, F., Gras, V., Guiot, J., Savarit, D., Blouin, P., Zanusso, M., Clément, P., Brossaud, J., Fischer, I., Moineau, M. P., Kerspern, H., Andlauer, P., Gaeremynck, E., Berchiche, S., Barba, F., Lebrun, C., Terrier, N., Kemeny, S., Delevallée, C., Marceau, G., Gehrke, C., Lemaire, S., Ménégaut, L., Lefaure, G., Petit, V., Gauchez‐Quenin, A. S., Pavili, L., Chevallier‐Helas, F., Artur, F., Sigogneau, P., Groussin, H., Renom, G., Lepers, S., Chianéa, T., Veyrat, B., Le Querler, L., Martin‐Denavit, T., Sault, C., Galland, A., Cheillan, D., Brechard, M. P., Yerokine, P., Levy‐Mozziconacci, A., Toga, C., Sainte‐Rose, M., Wasels, R., Aubertin, D., Rahil, H., Roucaute, T., Boulle, N., Solassol, J., Minery, M., Baillet, C., Dauch, P., Chevillon, I., Masson, D., Rotella, C. M., Barguil, Y., Duhin, M., Got, L., Lachgar, M., Druart, L., Ramirez, J. M., Lacroix, I., Brethome, B., Cassuto, G., Cohen‐Bacrie, M., Ternaux, F., Beaujard, M. P., Annette‐Reisch, M., Bounaud, M. P., Nowak, E., Dossot, J. M., Odaert, H., Quillard Murain, M., Descombes, G., Belot, G., Tisseur, B., Gouneaud, J., Louzier, C., Tosetti, F., Romain, S., Handwerk, L., Molignier, R., De Mas, P., Le Van, M., Estepa, B., Tang, K.

    Veröffentlicht in Prenatal diagnosis

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    Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish von Lin, Sheng-Jia, Barbalho, Patricia G., Kaiyrzhanov, Rauan, Maroofian, Reza, Petree, Cassidy, Severino, Mariasavina, Stanley, Valentina, Varshney, Pratishtha, Bahena, Paulina, Alzahrani, Fatema, Alhashem, Amal, Pagnamenta, Alistair T., Aubertin, Gudrun, Estrada-Veras, Juvianee I., Hernández, Héctor Adrián Díaz, Mazaheri, Neda, Oza, Andrea, Thies, Jenny, Renaud, Deborah L., Dugad, Sanmati, McEvoy, Jennifer, Sultan, Tipu, Pais, Lynn S., Tabarki, Brahim, Villalobos-Ramirez, Daniel, Rad, Aboulfazl, Ambrose, J.C., Arumugam, P., Bleda, M., Boardman-Pretty, F., Boustred, C.R., Brittain, H., Caulfield, M.J., Chan, G.C., Fowler, T., Giess, A., Hamblin, A., Henderson, S., Hubbard, T.J.P., Jackson, R., Jones, L.J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Leigh, S.E.A., Leong, I.U.S., Lopez, F.J., Maleady-Crowe, F., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A.C., O‘Donovan, P., Odhams, C.A., Patch, C., Perez-Gil, D., Pereira, M.B., Pullinger, J., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R.H., Siddiq, A., Sieghart, A., Smith, S.C., Sosinsky, A., Stuckey, A., Tanguy, M., Thomas, E.R.A., Thompson, S.R., Tucci, A., Walsh, E., Welland, M.J., Williams, E., Witkowska, K., Wood, S.M., Galehdari, Hamid, Ashrafzadeh, Farah, Sahebzamani, Afsaneh, Saeidi, Kolsoum, Torti, Erin, Elloumi, Houda Z., Mora, Sara, Palculict, Timothy B., Yang, Hui, Ben Fowler, Joshi, Manali, Behra, Martine, Burgess, Shawn M., Nath, Swapan K., Kenna, Margaret, Houlden, Henry, Karimiani, Ehsan Ghayoor, Zaki, Maha S., Haaf, Thomas, Alkuraya, Fowzan S., Gleeson, Joseph G., Varshney, Gaurav K.

    Veröffentlicht in Genetics in medicine

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