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Author/Creator Molina Gomes, D.

1. A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes. (12th February 2014)

Authors:
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.
Journal:
Prenatal diagnosis
Issue:
Volume 34:Number 5(2014:May)
Page Start:
424
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study. (5th April 2013)

Authors:
Marle, N.; Martinet, D.; Aboura, A.; Joly‐Helas, G.; Andrieux, J.; Flori, E.; Puechberty, J.; Vialard, F.; Sanlaville, D.; Fert Ferrer, S.; Bourrouillou, G.; Tabet, A.C.; Quilichini, B.; Simon‐Bouy, B.; Bazin, A.; Becker, M.; Stora, H.; Amblard, S.; Doco‐Fenzy, M.; Molina Gomes, D.
Journal:
Clinical genetics
Issue:
Volume 85:Number 3(2014:Mar.)
Page Start:
233
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗