-
Burgess, T, Brown, NJ, Stark, Z, Bruno, DL, Oertel, R, Chong, B, Calabro, V, Kornberg, A, Sanderson, C, Kelly, J, et al.
Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions.
American Journal of Medical Genetics Part A
164(1)
:
77 -86
2014
view publication
-
Brown, N, Burgess, T, Forbes, R, McGillivray, G, Kornberg, A, Mandelstam, S, Stark, Z.
5q31.3 Microdeletion syndrome: Clinical and molecular characterization of two further cases.
American Journal of Medical Genetics Part A
161(10)
:
2604 -2608
2013
view publication
-
Hynes, K, Tarpey, P, Dibbens, LM, Bayly, MA, Berkovic, SF, Smith, R, Raisi, ZA, Turner, SJ, Brown, NJ, Desai, TD, et al.
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.
Journal of Medical Genetics
47(3)
:
211
2010
view publication
-
Brown, NJ, Berkovic, SF, Scheffer, IE.
Vaccination, seizures and ‘vaccine damage’.
Current Opinion in Neurology
20(2)
:
181 -187
2007
view publication
-
Brown, N.
Letters to the Editor.
Journal of Paediatrics and Child Health
43(1‐2)
:
92 -92
2007
view publication