W. A. Symmans

McLeod neuroacanthocytosis: Genotype and phenotype

Adrian Danek, Justin P. Rubio, Luca Rampoldi et al. · Annals of Neurology · 2001 · 242 citations

Life Sciences, Genetics, Neurology +16

Localization of the McLeod locus (XK) within Xp21 by deletion analysis.

Corlee J. Bertelson, A.O. Pogo, Asok Chaudhuri et al. · PubMed · 1988 · 96 citations

Life Sciences, Genetics, Molecular Genetics +7

Elevated Serum Creatine Phosphokinase in Subjects with McLeod Syndrome

W. L. Marsh, Nina Marsh, Amy M. Moore et al. · Vox Sanguinis · 1981 · 58 citations

Medicine, Pathology, Physiology +13

Hereditary Acanthocytosis Associated with the McLeod Phenotype of the Kell Blood Group System

W. A. Symmans, C. S. Shepherd, W. L. Marsh et al. · British Journal of Haematology · 1979 · 56 citations

Medicine, Genetics, Hematology +16

Two de novo mutations in one β globin chain: Hemoglobin atlanta-coventry, β75 Leu→Pro and β141 Leu deleted

Stephen O. Brennan, D. Williamson, W. A. Symmans et al. · Hemoglobin · 1986 · 16 citations

Life Sciences, Genetics, Hematology +13