Items where authors include "Miedzybrodzka, Z."

Article

McVeigh, T.P., Monahan, K.J., Christopher, J. et al. (86 more authors) (2024) Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of Medical Genetics, 61 (7). pp. 707-715. ISSN 0022-2593

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

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836