M. Cooper

Homozygosity for autosomal dominant Marfan syndrome.

Y. Barash, D. Duksin, J. Chemke, 1984, Journal of medical genetics.

Familial mesangio-capillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome.

P. Mathieson, M. McGraw, D. J. Unsworth, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaic.

R. Hoffman, W. R. Breg, M. Cooper, 1984, Cancer genetics and cytogenetics.

Familial protein S deficiency is associated with recurrent thrombosis.

C. Esmon, P. Comp, R. Nixon, 1984, The Journal of clinical investigation.