S. Aslam

Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIIIA subunit

V. Yee, G. Standen, S. Narayanan, 1997, British journal of haematology.

Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.

G. Standen, S. Aslam, 1997, Postgraduate medical journal.

Factor XIIIA subunit deficiency due to a homozygous 13‐base pair deletion in exon 3 of the A subunit gene

D. Bowen, G. Standen, R. Gialeraki, 1996, American journal of hematology.

Factor XIIIA calgary: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIIIA subunit

V. Yee, M. Poon, D. Bowen, 1995, British journal of haematology.

Prenatal diagnosis in factor XIII-A deficiency

C. J. Barton, G. Standen, Caroline J Killick, 1999, Archives of disease in childhood. Fetal and neonatal edition.

The mutational frequency of BRAF and KRAS in low‐grade serous testicular neoplasms—a case series

J. Braybrooke, T. Clench, Z. Melegh, 2017, Histopathology.

A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit gene.

G. Standen, T. Mandalaki, R. Gialeraki, 1998, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.