K Michaelides

Moderation of hemophilia A phenotype by the factor V R506Q mutation

WC Nichols, Kagehiro Amano, PM Cacheris et al. · Blood · 1996 · 141 citations · Full text

Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndrome

SD Wright, K Michaelides, Johnson Dj et al. · Blood · 1993 · 103 citations · Full text

Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene

R. Michel, A. Lalloz, R. Schwaab et al. · British Journal of Haematology · 1994 · 78 citations

A G → A substitution in an HNF I binding site in the human α-fetoprotein gene is associated with hereditary persistence of α-fetoprotein (HPAFP)

John H. McVey, K Michaelides, Linda P. Hansen et al. · Human Molecular Genetics · 1993 · 74 citations

Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein

R. Schwaab, Johannes Oldenburg, M. R. A. LALLOZ et al. · Human Genetics · 1997 · 42 citations

Genetics, Pathogenesis, Hematology +4