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Author/Creator Van Maldergem, L

3. Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment. Issue 1 (13th May 2005)

Authors:
Janssens, K; Vanhoenacker, F; Bonduelle, M; Verbruggen, L; Van Maldergem, L; Ralston, S; Guañabens, N; Migone, N; Wientroub, S; Divizia, M T; Bergmann, C; Bennett, C; Simsek, S; Melançon, S; Cundy, T; Van Hul, W
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 1(2006)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Clinical, molecular, and genotype–phenotype correlation studies from 25 cases of oral–facial–digital syndrome type 1: a French and Belgian collaborative study. Issue 1 (5th January 2006)

Authors:
Thauvin-Robinet, C; Cossée, M; Cormier-Daire, V; Van Maldergem, L; Toutain, A; Alembik, Y; Bieth, E; Layet, V; Parent, P; David, A; Goldenberg, A; Mortier, G; Héron, D; Sagot, P; Bouvier, A M; Huet, F; Cusin, V; Donzel, A; Devys, D; Teyssier, J R
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 1(2006)
Page Start:
54
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. Issue 10 (1st October 2002)

Authors:
Van Maldergem, L; Magré, J; Khallouf, T E; Gedde-Dahl, T; Delépine, M; Trygstad, O; Seemanova, E; Stephenson, T; Albott, C S; Bonnici, F; Panz, V R; Medina, J-L; Bogalho, P; Huet, F; Savasta, S; Verloes, A; Robert, J-J; Loret, H; de Kerdanet, M; Tubiana-Rufi, N
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 10(2002)
Page Start:
722
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗