-
Peris, M, Reid, SM, Dobie, S, Bonacquisto, L, Shepherd, DA, Amor, DJ.
First‐trimester maternal serum biomarkers and the risk of cerebral palsy.
Developmental Medicine & Child Neurology
63(2)
:
183 -189
2021
view publication
-
Downie, L, Halliday, J, Burt, R, Lunke, S, Lynch, E, Martyn, M, Poulakis, Z, Gaff, C, Sung, V, Wake, M, et al.
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
European Journal of Human Genetics
29(2)
:
363 -363
2021
view publication
-
Kirk, EP, Ong, R, Boggs, K, Hardy, T, Righetti, S, Kamien, B, Roscioli, T, Amor, DJ, Bakshi, M, Chung, CWT, et al.
Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”).
European Journal of Human Genetics
29(1)
:
79 -87
2021
view publication
-
Wallis, M, Pope‐Couston, R, Mansour, J, Amor, DJ, Tang, P, Stock‐Myer, S.
Lymphedema distichiasis syndrome may be caused by FOXC2 promoter‐enhancer dissociation and disruption of a topological associated domain.
American Journal of Medical Genetics Part A
185(1)
:
150 -156
2021
view publication
-
Amor, DJ.
Fragile X Syndrome and Premutation Disorders: New Developments and Treatments Edited by Randi J Hagerman and Paul J Hagerman. London: Mac Keith Press, 2020. £75.00 (Hardback), pp 176. ISBN: 9781911612377.
Developmental Medicine & Child Neurology
63(1)
:
119 -119
2021
view publication