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190-kb duplication in 1p36.11 including PIGV and ARID1A genes in a girl with intellectual disability and hexadactyly.
Published in:
Clinical Genetics, 2013, v. 84, n. 6, p. 596, doi. 10.1111/cge.12113
By:
- Coutton, C;
- Bidart, M;
- Rendu, J;
- Devillard, F;
- Vieville, G;
- Amblard, F;
- Lopez, G;
- Jouk, P‐S;
- Satre, V
Publication type:
Article
Population screening for aneuploidy using maternal age and ultrasound.
Published in:
Prenatal Diagnosis, 1998, v. 18, n. 7, p. 683, doi. 10.1002/(SICI)1097-0223(199807)18:7<683::AID-PD327>3.0.CO;2-G
By:
- Cans, C.;
- Amblard, F.;
- Devillard, F.;
- Pison, H.;
- Jalbert, P.;
- Jouk, P. S.
Publication type:
Article
Erratum: Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells.
Published in:
Nature Cell Biology, 2014, v. 16, n. 4, p. 382, doi. 10.1038/ncb2946
By:
- Reay, M.;
- Parrini, M. C.;
- Cochet-Escartin, O.;
- Ladoux, B.;
- Buguin, A.;
- Coscoy, S.;
- Amblard, F.;
- Camonis, J.;
- Silberzan, P.
Publication type:
Article
Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells.
Published in:
Nature Cell Biology, 2014, v. 16, n. 3, p. 217, doi. 10.1038/ncb2917
By:
- Reffay, M.;
- Parrini, M. C.;
- Cochet-Escartin, O.;
- Ladoux, B.;
- Buguin, A.;
- Coscoy, S.;
- Amblard, F.;
- Camonis, J.;
- Silberzan, P.
Publication type:
Article
Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia.
Published in:
Human Reproduction, 2007, v. 22, n. 7, p. 1854, doi. 10.1093/humrep/dem127
By:
- A.K. Faure;
- I. Aknin-Seifer;
- V. Satre;
- F. Amblard;
- F. Devillard;
- S. Hennebicq;
- J. Chouteau;
- U. Bergues;
- R. Levy;
- S. Rousseaux
Publication type:
Article
A 140-Kilodalton Protein Is Released from Cultured Astrocytes by Phosphatidylinositol Phospholipase C.
Published in:
Journal of Neurochemistry, 1988, v. 50, n. 2, p. 486, doi. 10.1111/j.1471-4159.1988.tb02937.x
By:
- Amblard, F.;
- He, J.-T.;
- Barbet, J.;
- Goridis, C.;
- Prochiantz, A.
Publication type:
Article
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases.
Published in:
Prenatal Diagnosis, 2014, v. 34, n. 12, p. 1133, doi. 10.1002/pd.4439
By:
- Gruchy, N.;
- Vialard, F.;
- Blondeel, E.;
- Le Meur, N.;
- Joly‐Hélas, G.;
- Chambon, P.;
- Till, M.;
- Herbaut‐Graux, M.;
- Vigouroux‐Castera, A.;
- Coussement, A.;
- Lespinasse, J.;
- Amblard, F.;
- Jimenez, M.;
- Lebel Roy Camille, L.;
- Carré‐Pigeon, F.;
- Flori, E.;
- Mugneret, F.;
- Jaillard, S.;
- Yardin, C.;
- Harbuz, R.
Publication type:
Article
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 diagnosis of DMD in a female foetus affected by Turner syndrome.
Published in:
Prenatal Diagnosis, 2004, v. 24, n. 11, p. 913, doi. 10.1002/pd.1031
By:
- Satre, V.;
- Monnier, N.;
- Devillard, F.;
- Amblard, F.;
- Lunardi, Pr J.
Publication type:
Article
Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.
Published in:
Molecular Syndromology, 2014, v. 5, n. 1, p. 25, doi. 10.1159/000355391
By:
- Coutton, C.;
- Poreau, B.;
- Devillard, F.;
- Durand, C.;
- Odent, S.;
- Rozel, C.;
- Vieville, G.;
- Amblard, F.;
- Jouk, P.-S.;
- Satre, V.
Publication type:
Article

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