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Author/Creator Brueton, L A

5. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. Issue 9 (4th March 2009)

Authors:
Kleefstra, T; van Zelst-Stams, W A; Nillesen, W M; Cormier-Daire, V; Houge, G; Foulds, N; van Dooren, M; Willemsen, M H; Pfundt, R; Turner, A; Wilson, M; McGaughran, J; Rauch, A; Zenker, M; Adam, M P; Innes, M; Davies, C; López, A González-Meneses; Casalone, R; Weber, A
Journal:
Journal of medical genetics
Issue:
Volume 46:Issue 9(2009)
Page Start:
598
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes. Issue 6 (1st June 2004)

Authors:
Aldred, M A; Sanford, R O C; Thomas, N S; Barrow, M A; Wilson, L C; Brueton, L A; Bonaglia, M C; Hennekam, R C M; Eng, C; Dennis, N R; Trembath, R C
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 6(2004)
Page Start:
433
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗