Variability in the fetal hemoglobin level of the normal adultJ.Ye. Leonova, Titus H.J. Huisman, Georgi D. Efremov et al.|American Journal of Hematology|1996Cited by 40
Co-Inheritance of Hb D-PUNJAB (CODON 121; GAA→CAA) and β0-Thalassemia (IVS-II-1; G→A)Adekunle Adekile, T. H. J. Huisman, E. G. Kazanetz et al.|Journal of Pediatric Hematology/Oncology|1996Cited by 16
A de novo Deletion Causing εγδβ-Thalassemia in a Dutch PatientJ. Abels, T. H. J. Huisman, J. J. Michiels et al.|Acta Haematologica|2009Cited by 13
β-Thalassemia Intermedia in An Indian Female h the Hb Hofu [β126(H4)Val→Glu]-(β°-Thalassemia [Codons 8/9 (+G)] CombinationP.L. Pande, T. H. J. Huisman, Satya Prakash et al.|Hemoglobin|1995Cited by 8
Hb ananosa or α<sub>2</sub>111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α<sub>2</sub>123(H6)Ala → Serβ<sub>2</sub>(αl Mutation) are two silent stable variants detected by sequencing of amplified dnaE. G. Kazanetz, T. H. J. Huisman, J.Ye. Leonova et al.|Hemoglobin|1995Cited by 7