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Proceedings of the National Academy of Sciences of the United States of America|December 13, 2002
Genetic variation in the 22q11 locus and susceptibility to schizophreniaHui Liu, Goncalo R Abecasis, Simon C Heath, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 11, 2022
Diagnostic performance of dobutamine stress echocardiography: A South African experienceL Scherman, C Cilliers, D Odendaal, et al.
American Journal of Human Genetics|January 30, 2004
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Gonçalo R Abecasis, Rachel A Burt, Diana Hall, et al.
American Journal of Medical Genetics. Part A|May 2, 2015
The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defectsYaojuan Jia, Jacoba J Louw, Jeroen Breckpot, et al.
Plos One|November 29, 2007
Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approachesRuby Hsu, Abigail Woodroffe, Wen-Sung Lai, et al.
Leukemia & Lymphoma|December 23, 2022
The International Prognostic Score and HIV status predict red cell concentrate transfusion needs in Hodgkin lymphomaKudakwashe Simba, Zainab Mohamed, Jessica J Opie, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2002
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophreniaHui Liu, Simon C Heath, Christina Sobin, et al.
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