Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations by Rumaney, Maryam

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Knowledge and experiences of parents with children affected by Sickle Cell Disease in Cape Town by Van Niekerk, Katryn

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Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease by Pule, Gift Dineo

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Parents' perspectives and experiences of having a child with hereditary hearing loss by Ross, Sinead Amber

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Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon by Geard, Amy

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Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing by Ngongang Tekendo, Cedrik

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Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa by Ingram, Clair

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Whole exome sequencing to investigate genetic variants of non-syndromic hearing impairment in a population of African ancestry by Manyisa, Noluthando

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Genetic aetiology of autosomal recessive non-syndromic hearing loss in sub-Saharan African patients: evaluation using targeted and whole exome sequencing by Lebeko, Kamogelo

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Significance of connexion genes in non-syndromic deafness in Africans by Bosch, Jason

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Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort by Masekoameng, Tshepiso

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Return of a Fragile X Syndrome Genetic Result: Exploring the feedback of Individual genetic findings and their relation to traditional knowledge in a village in Cameroon by Karen, Kengne Kamga

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Pharmacogenomics of sickle cell disease therapeutics: pain and drug metabolism associated gene variants and hydroxyurea-induced post-transcriptional expression of miRNAs by Mnika,Khuthala

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Genetics of hearing impairment and peripheral neuropathy in Mali by Yalcouye, Abdoulaye

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The genetics of non-syndromic hearing impairment in South Africa by Manyisa, Noluthando

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Genomics of sickle cell disease and fetal hemoglobin in African populations by Esoh, Kum Kevin

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Risk factors associated with blood pressure variation in sickle cell disease in Cameroon by Nguweneza, Arthemon

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