Items where authors include "O’Driscoll, M."

Article

Lee, S.L. orcid.org/0000-0003-2806-3268, Foster, A., May, D. orcid.org/0009-0003-1850-6595 et al. (12 more authors) (2025) Familial NSD1 exon 3 deletion associated with phenotypic and epigenetic variability. Genes, 16 (10). 1190. ISSN 2073-4425

Piña-Aguilar, R., Simpson, S.A., Alshatti, A. et al. (17 more authors) (2019) 27 years of prenatal diagnosis for Huntington disease in the United Kingdom. Genetics in Medicine, 21 (7). pp. 1639-1643. ISSN 1098-3600

Quarrell, O.W., Clarke, A.J., Compton, C. et al. (14 more authors) (2018) Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 177 (1). pp. 35-39. ISSN 1552-4841