G. Yawson

The Second Variant of Human Myoglobin; 138 (H16) Arginine → Glutamine

H. Lehmann, P. Lorkin, F. Boulton, 1971 .

Abnormal haemoglobins in 4,000 blood donors at Korle Bu.

G. Yawson, E. Marbell, B. B. Tribedi, 1973 .

An automated screening technique for the detection of sickle-cell haemoglobin

R. Huntsman, G. Yawson, D. Canning, 1972, Journal of clinical pathology.

A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anaemia

R. Huntsman, G. Yawson, G. Barclay, 1970, Journal of clinical pathology.

THE USE OF THE CORD BLOOD SAMPLE FOR THE DETECTION OF SICKLE‐CELL ANAEMIA IN THE NEWBORN

R. Huntsman, G. Yawson, J. Metters, 1970, The Journal of obstetrics and gynaecology of the British Commonwealth.

An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples

R. Huntsman, G. Yawson, J. Metters, 1970, Journal of clinical pathology.

Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at Birth

T. Huisman, B. Ringelhann, F. Konotey-Ahulu, 1977, Pediatric Research.

Homozygotes for the hereditary persistence of fetal hemoglobin: The ratio of Gγ to Aγ chains and biosynthetic studies

T. Huisman, W. Schroeder, B. Ringelhann, 1977, Biochemical Genetics.

The diagnosis of sickle cell disease in the newborn infant.

R. Huntsman, G. Yawson, J. Metters, 1972, The Journal of pediatrics.