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You searched for: Author/Creator Atoyebi, Wale

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1. A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias. (19th July 2016)

2. Paediatric to adult transition care for patients with sickle cell disease: a global perspective. Issue 4 (April 2020)

3. Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic. (10th May 2020)

4. Sequence analysis of exon 1 of the ferritin light chain (FTL) gene can reveal the rare disorder 'hereditary hyperferritinaemia without cataracts'. (23rd May 2018)