Works matching IS 01973851 AND DT 2014 AND VI 34 AND IP 5


Results: 16
    1
    2

    De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.

    Published in:
    Prenatal Diagnosis, 2014, v. 34, n. 5, p. 460, doi. 10.1002/pd.4330
    By:
    • Malvestiti, Francesca;
    • De Toffol, Simona;
    • Grimi, Beatrice;
    • Chinetti, Sara;
    • Marcato, Livia;
    • Agrati, Cristina;
    • Di Meco, Anna Maria;
    • Frascoli, Giuditta;
    • Trotta, Anna;
    • Malvestiti, Barbara;
    • Ruggeri, Anna;
    • Dulcetti, Francesca;
    • Maggi, Federico;
    • Simoni, Giuseppe;
    • Grati, Francesca Romana
    Publication type:
    Article
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15

    A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.

    Published in:
    Prenatal Diagnosis, 2014, v. 34, n. 5, p. 424, doi. 10.1002/pd.4321
    By:
    • Besseau‐Ayasse, J.;
    • Violle‐Poirsier, C.;
    • Bazin, A.;
    • Gruchy, N.;
    • Moncla, A.;
    • Girard, F.;
    • Till, M.;
    • Mugneret, F.;
    • Coussement, A.;
    • Pelluard, F.;
    • Jimenez, M.;
    • Vago, P.;
    • Portnoï, M. F.;
    • Dupont, C.;
    • Beneteau, C.;
    • Amblard, F.;
    • Valduga, M.;
    • Bresson, J. L.;
    • Carré‐Pigeon, F.;
    • Le Meur, N.
    Publication type:
    Article
    16