-
Kraan, CM, Date, P, Rattray, A, Sangeux, M, Bui, QM, Baker, EK, Morison, J, Amor, DJ, Godler, DE.
Feasibility of wearable technology for 'real-world' gait analysis in children with Prader-Willi and Angelman syndromes..
J Intellect Disabil Res
66(8-9)
:
717 -725
2022
view publication
-
Baker, EK, Merton, CF, Tan, W-H, Dudding-Byth, T, Godler, DE, Sadhwani, A.
Methylation analysis and developmental profile of two individuals with Angelman syndrome due to mosaic imprinting defects..
Eur J Med Genet
65(4)
:
104456
2022
view publication
-
Godler, DE, Ling, L, Gamage, D, Baker, EK, Bui, M, Field, MJ, Rogers, C, Butler, MG, Murgia, A, Leonardi, E, et al.
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow..
JAMA Netw Open
5(1)
:
e2141911
2022
view publication
-
Bartlett, E, Archibald, AD, Francis, D, Ling, L, Thomas, R, Chandler, G, Ward, L, O'Farrell, G, Pandelache, A, Delatycki, MB, et al.
Paternal retraction of a fragile X allele to normal size, showing normal function over two generations..
Am J Med Genet A
188(1)
:
304 -309
2022
view publication
-
Richdale, AL, Baker, EK, Sciberras, E.
Sleep in Children with Neurodevelopmental Disorders.
193 -209
2022
view publication