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Genome Research|May 1, 1997
A 1.1-Mb transcript map of the hereditary hemochromatosis locusD A Ruddy, G S Kronmal, V K Lee, et al.
Molecular Genetics and Metabolism|January 9, 2010
Clinical experience with miglustat therapy in pediatric patients with Niemann-Pick disease type C: a case seriesM Pineda, M S Perez-Poyato, M O'Callaghan, et al.
Health Promotion and Chronic Disease Prevention in Canada : Research, Policy and Practice|June 12, 2025
Global prevalence of post-COVID-19 condition: a systematic review and meta-analysis of prospective evidenceMohamed Kadry Taher, Talia Salzman, Allyson Banal, et al.
Health Promotion and Chronic Disease Prevention in Canada : Research, Policy and Practice|March 12, 2025
Global prevalence of post-COVID-19 condition: a systematic review and meta-analysis of prospective evidenceMohamed Kadry Taher, Talia Salzman, Allyson Banal, et al.
JAMA Neurology|February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystoniaKishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Revista De Neurologia|April 2, 1999
[Rett's syndrome in the Spanish population]M Pineda, A Aracil, A Vernet, et al.
Nature Genetics|August 1, 1996
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisJ N Feder, A Gnirke, W Thomas, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|September 22, 2025
May Measurement Month 2022: an analysis of blood pressure screening results from PhilippinesArnold Benjamin C Mina, Neil R Poulter, Thomas Beaney, et al.
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