Arab Genetic Disease Database (AGDDB): A population-specific clinical and mutation database

Human Mutation

Volumn 19, Issue 6, 2002, Pages 615-621

  Teebi, Ahmad S ^a   Teebi, Saeed A ^a   Porter, Christopher J ^a   Cuticchia, A Jamie ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Arab Genetic Disease Consortium; Arabs; Clinical; Database; Diversity; Genetic disorders; Mutation analysis; Population

Indexed keywords

ARAB; DATA BASE; GENE MUTATION; GENETIC DISORDER; HUMAN; POPULATION GENETICS; POPULATION RESEARCH; PRIORITY JOURNAL; REVIEW;

ARABS; DATABASES, GENETIC; GENETIC DISEASES, INBORN; GENETICS, POPULATION; HUMANS; MUTATION;

EID: 0036261479     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10082     Document Type: Review

References (15)

1. Recommendations for a nomenclature system for human gene mutations
2. Cystic fibrosis and the Gulf states
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4. Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: Evidence for founder effect and genomic recombination at the CA II locus
5. Recent advances in molecular genetics of the Maghreb and the Middle East populations: The first Middle East genetics association of America (MEGA) conference
6. Genetic referrals of Middle Eastern origin in a western city: Inbreeding and disease profile
7. Metabolic alkalosis in cystic fibrosis: Atypical presentation in Kuwait
8. Distribution of CFTR mutations on cystic fibrosis patients of Tunisian origin: Identification of two novel mutations
9. Opitz G/BBB syndrome: Clinical comparisons of families linked to Xp22 and 22q, and review of the literature
10. PAHdb: A locus-specific knowledge base
11. Autosomal recessive disorders among Arabs: An overview from Kuwait
12. Population and molecular genetic update; the second Middle East genetic association of America (MEGA) conference