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Molecular Genetics & Genomic Medicine|June 13, 2020
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutationBronwyn Dillon, Candice Feben, David Segal, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 23, 2003
Investigation of the normal proximal somatomotor system using magnetoencephalographyJulia M Stephen, Larry E Davis, Cheryl J Aine, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|December 5, 2013
Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutationTasha Wainstein, Robyn Kerr, Claire L Mitchell, et al.Cancer|July 27, 2004
Hepatocellular carcinoma and liver tumors in South African children: a case for increased prevalenceSamuel W Moore, Alistair J W Millar, G P Hadley, et al.Journal of Pediatric Hematology/Oncology|February 21, 2014
Malignancies in South African children with HIVAlan Davidson, Rosalinda D Wainwright, David K Stones, et al.Diagnostic Cytopathology|August 14, 2012
An interinstitutional review of the value of FNAB in pediatric oncology in resource-limited countriesRubina Razack, Pamela Michelow, Gladwyn Leiman, et al.Pediatric Blood & Cancer|January 23, 2021
Age at diagnosis as a prognostic factor in South African children with neuroblastomaJaques van Heerden, Tonya M Esterhuizen, Marc Hendricks, et al.DNA Repair|November 21, 2017
Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronucleiFlavia Zita Francies, Rosalind Wainwright, Janet Poole, et al.Blood|January 20, 2005
A common Fanconi anemia mutation in black populations of sub-Saharan AfricaNeil V Morgan, Fahmida Essop, Ilja Demuth, et al.JCO Global Oncology|August 29, 2024
Outcome of Retinoblastoma After Implementation of National Retinoblastoma Treatment Guidelines in South AfricaMariana Kruger, Sabine L van Elsland, Alan Davidson, et al.Pageof 3