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British Journal of Haematology|December 3, 1999
The erythrocyte effects of haemoglobin O(ARAB)R L Nagel, R Krishnamoorthy, S Fattoum, et al.
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Diabetologia|March 1, 1990
HLA-DQB 1 codon 57 and genetic susceptibility to type 1 (insulin-dependent) diabetes mellitus in French childrenI Vallet-Colom, C Lévy-Marchal, D Zarrouk, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.
Human Genetics|August 1, 1988
DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterizationF Rouabhi, C Lapouméroulie, S Amselem, et al.
British Journal of Haematology|February 1, 1996
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemiasC Guidal-Giroux, B Gérard, H Cavé, et al.
American Journal of Hematology|July 1, 1992
Genetic epidemiology of beta-thalassemia in Sicily: do sequences 5' to the G gamma gene and 5' to the beta gene interact to enhance HbF expression in beta-thalassemia?A Ragusa, M Lombardo, C Beldjord, et al.
Infection and Immunity|January 23, 1999
The link between phylogeny and virulence in Escherichia coli extraintestinal infectionB Picard, J S Garcia, S Gouriou, et al.
Fetal Diagnosis and Therapy|September 1, 1993
Measurement of adult hemoglobin in fetal blood samples by high-performance liquid chromatography as purity control for the prenatal diagnosis of chromosomal abnormalitiesR Ducrocq, G Tachdjian, J F Oury, et al.
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