M. R. A. LALLOZ

Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping

Mina Ohadi, M. R. A. LALLOZ, Pak C. Sham et al. · The American Journal of Human Genetics · 1999 · 216 citations · Full text

Mendelian Disorder, Health Sciences, Cytogenetics +12

Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

M. R. A. LALLOZ · The Lancet · 1991 · 140 citations

Genetics, Pathogenesis, Hematology +5

Rapid Identification of Hemoglobin Variants by Electrospray Ionization Mass Spectrometry

Barbara Wild, B.N. Green, Elaine Cooper et al. · Blood Cells Molecules and Diseases · 2001 · 121 citations

Laboratory Hematology, Biochemistry, Natural Sciences +10

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

Christian Datz, M. R. A. LALLOZ, W. Vogel et al. · Journal of Hepatology · 1997 · 83 citations

Haplotype Determination, Mendelian Disorder, Genetic Disorder +11

Genetic and acquired predisposing factors and treatment of osteoporosis in thalassaemia major.

B. Wonke, C. E. Jensen, J J Hanslip et al. · PubMed · 1998 · 74 citations

Bone Disease, Sclerostin, Bone Health +15