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Loesch, DZ, Cook, M, Litewka, L, Gould, E, Churchyard, A, Tassone, F, Slater, HR, Storey, E.
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.
Journal of Medical Genetics
45(3)
:
179
2008
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Bruno, DL, Burgess, T, Ren, H, Nouri, S, Pertile, MD, Francis, DI, Norris, F, Kenney, BK, Schouten, J, Choo, KHA, et al.
High‐throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy.
American Journal of Medical Genetics Part A
140A(24)
:
2786 -2793
2006
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Kannu, P, Oei, P, Slater, HR, Khammy, O, Aftimos, S.
Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome.
American Journal of Medical Genetics Part A
140A(18)
:
1955 -1959
2006
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Slater, HR, Bailey, DK, Ren, H, Cao, M, Bell, K, Nasioulas, S, Henke, R, Choo, KHA, Kennedy, GC.
Reply to Wirtenberger et al..
American Journal of Human Genetics
78(4)
:
730 -731
2006
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Loesch, DZ, Bui, QM, Kelso, W, Huggins, RM, Slater, H, Warne, G, Bergman, PB, Rodda, C, Mitchell, RJ, Prior, M.
Corrigendum to “Effect of Turner's syndrome and X-linked imprinting on cognitive status: Analysis based on pedigree data” [Brian Dev. 27 (2005) 494–503]☆.
Brain and Development
28(2)
:
134
2006
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