Browse by Supervisor

Fütterer, Jane Wong (2017). Characterisation of a novel protein, ANKRD18A, implicated in a severe form of thrombocytopenia. University of Birmingham. Ph.D.

Alsaedi, Atif Saud (2017). Exome sequencing analysis of rare autosomal recessive disorders. University of Birmingham. Ph.D.

Almazni, Ibrahim (2021). Identification and functional investigation of genes in patients with inherited bleeding disorders. University of Birmingham. Ph.D.

Maclachlan, Annabel Elizabeth Nicol (2020). Identification and functional investigation of genes involved in inherited bleeding disorders. University of Birmingham. Ph.D.

Khan, Abdullah O. (2019). Investigating the molecular causes of inherited thrombocytopenia using CRISPR-Cas9 gene editing and super-resolution microscopy. University of Birmingham. Ph.D.

Stapley, Rachel J. (2021). Investigating the role of SLFN14 mutations in inherited thrombocytopenia and haematopoiesis. University of Birmingham. Ph.D.

Johnson, Ben David (2017). Molecular genetic investigation into inherited thrombocytopenia. University of Birmingham. Ph.D.

Colley, Emily Charlotte (2021). The investigation of cell free DNA and genetic causes in the evaluation of miscarriage. University of Birmingham. Ph.D.

Johnson, Ben (2013). Utilising the zebrafish model organism to study the effect of FLCN in early embryonic development and Genotyping and platelet phenotyping of cases of rare inherited platelet based bleeding disorders. University of Birmingham. M.Res.