Search

Author/Creator Moutard, M L

1. A second locus for Aicardi-Goutières syndrome at chromosome 13q14–21. Issue 5 (20th May 2005)

Authors:
Ali, M; Highet, L J; Lacombe, D; Goizet, C; King, M D; Tacke, U; van der Knaap, M S; Lagae, L; Rittey, C; Brunner, H G; van Bokhoven, H; Hamel, B; Oade, Y A; Sanchis, A; Desguerre, I; Cau, D; Mathieu, N; Moutard, M L; Lebon, P; Kumar, D
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 5(2006)
Page Start:
444
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22. Issue 3 (March 1997)

Authors:
des Portes, V; Pinard, J M; Smadja, D; Motte, J; Boespflüg-Tanguy, O; Moutard, M L; Desguerre, I; Billuart, P; Carrie, A; Bienvenu, T; Vinet, M C; Bachner, L; Beldjord, C; Dulac, O; Kahn, A; Ponsot, G; Chelly, J
Journal:
Journal of medical genetics
Issue:
Volume 34:Issue 3(1997)
Page Start:
177
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search