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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
Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Published in:
Prenatal Diagnosis, 2005, v. 25, n. 6, p. 451, doi. 10.1002/pd.1154
By:
- Beaujard, M.-P.;
- Jouannic, J.-M.;
- Bessières, B.;
- Borie, C.;
- Martin-Luis, I.;
- Fallet-Bianco, C.;
- Portnoï, M.-F.
Publication type:
Article