B. Serjeant

Improved survival in homozygous sickle cell disease: lessons from a cohort study

G. Serjeant, B. Serjeant, P. Thomas, 1995, BMJ.

Heights and weights of Jamaican children with homozygous sickle cell disease.

G. Serjeant, M. T. Ashcroft, P. Desai, 1977, Human biology.

Retained Splenic Function in an Indian Population with Homozygous Sickle Cell Disease May Have Important Clinical Significance

I. Hambleton, G. Serjeant, B. Serjeant, 2021, Indian journal of community medicine : official publication of Indian Association of Preventive & Social Medicine.

Determinants of Haemoglobin Level in Sickle Cell‐Haemoglobin C Disease

J. England, G. Serjeant, M. Seakins, 1979, British journal of haematology.

Red cell antibodies in patients with homozygous sickle cell disease: a comparison of patients in Jamaica and the United Kingdom

I. Hambleton, G. Serjeant, B. Serjeant, 2001, British journal of haematology.

Determinants of haemoglobin level in steady‐state homozygous sickle cell disease

D. Higgs, D. Higgs, G. Serjeant, 1996, British journal of haematology.

The clinical significance of serum transferrin receptor levels in sickle cell disease

J. Cook, B. Skikne, A. Singhal, 1993, British journal of haematology.