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Journal of Affective Disorders|July 23, 2020
Whole-exome sequencing in an Afrikaner family with bipolar disorderHannah-Ruth Engelbrecht, Shareefa Dalvie, Gloudi Agenbag, et al.Journal of Ethnopharmacology|April 9, 2008
The in vivo effects of Tulbhagia violacea on blood pressure in a salt-sensitive rat modelIrene Mackraj, S Ramesar, M Singh, et al.Investigative Ophthalmology & Visual Science|November 30, 2016
Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome SequencingLisa Roberts, Rinki Ratnapriya, Morné du Plessis, et al.American Journal of Medical Genetics|October 1, 1990
Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagenI J Anderson, P Tsipouras, C Scher, et al.Bipolar Disorders|May 3, 2008
Neuropsychological task performance in bipolar spectrum illness: genetics, alcohol abuse, medication and childhood traumaJonathan B Savitz, Lize van der Merwe, Dan J Stein, et al.Journal of Medical Genetics|June 1, 1996
Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneityR S Ramesar, J Greenberg, R Martin, et al.Diseases of the Colon and Rectum|October 27, 1998
In a resource-poor country, mutation identification has the potential to reduce the cost of family management for hereditary nonpolyposis colorectal cancerP A Goldberg, M V Madden, C Harocopos, et al.Pharmacogenomics|November 21, 2014
Genetic variation in Otos is associated with cisplatin-induced ototoxicityTimothy F Spracklen, Heather Whitehorn, Anna Alvera Vorster, et al.American Journal of Industrial Medicine|November 17, 2017
DNA variants and organophosphate neurotoxicity among emerging farmers in the Western Cape of South AfricaTracy Glass, Mohamed A Dalvie, Zelda Holtman, et al.Mutation Research|November 8, 2006
GSTM1 and GSTT1 polymorphisms as modifiers of age at diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) in a homogeneous cohort of individuals carrying a single predisposing mutationRebecca Felix, Walter Bodmer, Nicola S Fearnhead, et al.Pageof 9