Peter van Delft

Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi‐ethnic populations

Peter van Delft, Egbert Lenters, Margreet Bakker‐Verweij et al. · International Journal of Laboratory Hematology · 2009 · 127 citations

Genetic Epidemiology, Diagnosis, Pathology +22

Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects

Cornelis L. Harteveld, Majid Yavarian, Amine Zoraï et al. · American Journal of Hematology · 2003 · 81 citations · Full text

Alpha-thalassemia Mutations, Allelic Variant, Haplotype Determination +13

Known and new delta globin gene mutations and their diagnostic significance.

Marelle J. Bouva, Cornelis L. Harteveld, Peter van Delft et al. · PubMed · 2006 · 48 citations

Mendelian Disorder, Genetic Disorder, Delta-globin Gene +13

MOLECULAR SPECTRUM OF<i>α</i>-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH

Amine Zoraï, Cornelis L. Harteveld, Achech Bakir et al. · Hemoglobin · 2002 · 35 citations

Genetic Testing, Variant Interpretation, Medicine +15

Haemoglobinopathy analyses in the Netherlands: a report of an <i>in vitro</i> globin chain biosynthesis survey using a rapid, modified method

Paola Giordano, Peter van Delft, D. Batelaan et al. · Clinical & Laboratory Haematology · 1999 · 33 citations

Laboratory Hematology, Biochemistry, Medicine +12