Research articles
Genetic diseases in Arab populations
Counselling about genetic disease: an Islamic perspective
Spectrum of genetic disorders and the impact on health care delivery: an introduction
Review of the spectrum of genetic diseases in Bahrain
Preventive aspects of genetic morbidity: experiences of the Canadian model
Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia
Haplotypes of the b-globin gene as prognostic factors in sickle-cell disease
Pattern for a-thalassaemia in Yemeni sickle-cell-disease patients
Prevalence of thalassaemia in schoolchildren in north-eastern Badia, Jordan
Haemostatic disorders in nonsplenectomized and splenectomized thalassaemic children
Communicating basic genetics to patients with sickle-cell disease
Molecular studies on Yemeni sickle-cell-disease patients: Xmn I polymorphism
Spectrum of hereditary coagulation factor deficiencies in Eastern Province, Saudi Arabia
Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response
Glutathione reductase deficiency in Saudi Arabia
Biotinidase deficiency: a treatable genetic disorder in the Saudi population
Use of FISH technique in the diagnosis of chromosomal syndromes
Application of DNA-based tests for diagnosis of spinal muscular atrophy in Saudi Arabia
Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia
Diabetes mellitus, hypertension and obesity — common multifactorial disorders in Saudis