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Godler, DE, Amor, DJ. DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders..
Essays in Biochemistry
63(6)
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785 -795
2019
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Prawer, Y, Hunter, M, Cronin, S, Ling, L, Vera, SA, Fahey, M, Gelfand, N, Oertel, R, Bartlett, E, Francis, D, et al. Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.
Genes
9(6)
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287
2018
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Hartin, SN, Hossain, WA, Francis, D, Godler, DE, Barkataki, S, Butler, MG. Analysis of the Prader–Willi syndrome imprinting center using droplet digital PCR and next‐generation whole‐exome sequencing.
Molecular Genetics & Genomic Medicine
7(4)
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e00575
2019
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Stark, Z, Francis, D, Gaffney, L, Greenberg, J, Hills, L, Li, X, Godler, DE, Slater, HR. Prenatal diagnosis of fragile X syndrome complicated by full mutation retraction.
American Journal of Medical Genetics Part A
167(10)
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2485 -2487
2015
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Cvejic, RC, Hocking, DR, Wen, W, Georgiou-Karistianis, N, Cornish, KM, Godler, DE, Rogers, C, Trollor, JN. Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome.
Brain Imaging and Behavior
13(4)
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1128 -1134
2018
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