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Author/Creator Mathieu, M

4. Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families. Issue 12 (29th July 2009)

Authors:
Willems, M; Geneviève, D; Borck, G; Baumann, C; Baujat, G; Bieth, E; Edery, P; Farra, C; Gerard, M; Héron, D; Leheup, B; Le Merrer, M; Lyonnet, S; Martin-Coignard, D; Mathieu, M; Thauvin-Robinet, C; Verloes, A; Colleaux, L; Munnich, A; Cormier-Daire, V
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 12(2010)
Page Start:
797
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech. Issue 6 (3rd June 2010)

Authors:
Bonnet, C; Andrieux, J; Béri-Dexheimer, M; Leheup, B; Boute, O; Manouvrier, S; Delobel, B; Copin, H; Receveur, A; Mathieu, M; Thiriez, G; Le Caignec, C; David, A; de Blois, M C; Malan, V; Philippe, A; Cormier-Daire, V; Colleaux, L; Flori, E; Dollfus, H
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 6(2010)
Page Start:
377
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗