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Author/Creator Coutton, C.

1. Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?. Issue 4 (16th February 2017)

Authors:
El Chehadeh, S.; Touraine, R.; Prieur, F.; Reardon, W.; Bienvenu, T.; Chantot‐Bastaraud, S.; Doco‐Fenzy, M.; Landais, E.; Philippe, C.; Marle, N.; Callier, P.; Mosca‐Boidron, A.‐L.; Mugneret, F.; Le Meur, N.; Goldenberg, A.; Guerrot, A.‐M.; Chambon, P.; Satre, V.; Coutton, C.; Jouk, P.‐S.
Journal:
Clinical genetics
Issue:
Volume 91:Issue 4(2017)
Page Start:
576
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study. (5th December 2018)

Authors:
Egloff, M.; Hervé, B.; Quibel, T.; Jaillard, S.; Le Bouar, G.; Uguen, K.; Saliou, A.‐H.; Valduga, M.; Perdriolle, E.; Coutton, C.; Coston, A.‐L.; Coussement, A.; Anselem, O.; Missirian, C.; Bretelle, F.; Prieur, F.; Fanget, C.; Muti, C.; Jacquemot, M.‐C.; Beneteau, C.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 52:Number 6(2018)
Page Start:
715
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗