Authors:
Kayser, M
Krawczak, M
Excoffier, L
Dieltjes, P
Corach, D
Pascali, V
Gehrig, C
Bernini, LF
Jespersen, J
Bakker, E
Roewer, L
de Knijff, P
Citation: M. Kayser et al., An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations, AM J HU GEN, 68(4), 2001, pp. 990-1018
Authors:
Kerkhoffs, JL
Harteveld, CL
Wijermans, P
van Delft, P
Haak, HL
Bernini, LF
Giordano, PC
Citation: Jl. Kerkhoffs et al., Very mild pathology in a case of Hb S/beta(0)-thalassemia in combination with a homozygosity for the alpha-thalassemia 3.7 kb deletion, HEMOGLOBIN, 24(3), 2000, pp. 259-263
Authors:
Harteveld, CL
Beijer, C
van Delft, P
Zanardini, R
Bernini, LF
Giordano, PC
Citation: Cl. Harteveld et al., alpha-Thalassaemia as a result of a novel splice donor site mutation of the alpha(1)-globin gene, BR J HAEM, 110(3), 2000, pp. 694-698
Authors:
Giordano, PC
Harteveld, CL
Bok, LA
van Delft, P
Batelaan, D
Beemer, FA
Bernini, LF
Citation: Pc. Giordano et al., A complex haemoglobinopathy diagnosis in a family with both beta(0)- and alpha(0/+)-thalassaemia homozygosity, EUR J HUM G, 7(2), 1999, pp. 163-168
Authors:
Van Weel, M
Harteveld, CL
Bernini, LF
Brouwers, TM
Giordano, PC
Citation: M. Van Weel et al., The second case of dominant beta-thalassemia induced by the codon 127 (CAG-> TAG) described as a De Novo mutation in a Dutch boy, HEMOGLOBIN, 23(4), 1999, pp. 389-393
Authors:
van den Berg, HM
Bruin, MCA
Batelaan, D
van Delft, P
van Zwieten, R
Roos, D
Harteveld, CL
Bernini, LF
Giordano, PC
Citation: Hm. Van Den Berg et al., Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl, HEMOGLOBIN, 23(2), 1999, pp. 135-144
Authors:
Giordano, PC
Van Delft, P
Batelaan, D
Harteveld, CL
Bernini, LF
Citation: Pc. Giordano et al., Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method, CLIN LAB H, 21(4), 1999, pp. 247-255
Authors:
Giordano, PC
Harteveld, CL
Michiels, JJ
Terpstra, W
Schelfhout, LJDM
Appel, IM
Batelaan, D
van Delft, P
Plug, RJ
Bernini, LF
Citation: Pc. Giordano et al., Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G -> T) mutation, ANN HEMATOL, 77(6), 1998, pp. 249-255