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Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 2014
Malformation risks of antiepileptic drug monotherapies in pregnancy: updated results from the UK and Ireland Epilepsy and Pregnancy RegistersE Campbell, F Kennedy, A Russell, et al.
Journal of Medical Genetics|April 4, 2006
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndromeN C M Hearle, M F Rudd, W Lim, et al.
Seizure|July 17, 2021
Zonisamide safety in pregnancy: Data from the UK and Ireland epilepsy and pregnancy registerG McCluskey, M O Kinney, A Russell, et al.
Journal of Medical Genetics|March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational studyOliver W J Quarrell, Alan S Rigby, L Barron, et al.
Journal of Medical Genetics|November 11, 2008
Risk reducing mastectomy: outcomes in 10 European centresD G R Evans, A D Baildam, E Anderson, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 19, 2022
Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genesC Loveday, A Garrett, P Law, et al.
Clinical and Experimental Immunology|July 12, 2013
The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008-2012J D M Edgar, M Buckland, D Guzman, et al.
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