Showing 31–40 of 51 publications
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ORCID
Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania
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ORCID
The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies
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ORCID
The International Hemoglobinopathy Research Network (INHERENT): An International Initiative to Study the Role of Genetic Modifiers in Hemoglobinopathies
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ORCID
Perspectives on Building Sustainable Newborn Screening Programs for Sickle Cell Disease: Experience from Tanzania
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ORCID
Influence of gender norms in relation to child's quality of care: follow-up of families of children with SCD identified through NBS in Tanzania
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ORCID
Inauguration of the Tanzania Society of Human Genetics: Biomedical Research in Tanzania with Emphasis on Human Genetics and Genomics
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ORCID
Hematological and Biochemical Reference Ranges for Population With Sickle Cell Disease at Steady-State in Tanzania
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ORCID
A Baseline Evaluation of Bioinformatics Capacity in Tanzania Reveals Areas for Training
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ORCID
Baseline Evaluation of Bioinformatics Capacity in Tanzania
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ORCID
F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease
