Arab genetic disease database (AGDDB): A population-specific clinical and mutation database
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference15 articles.
1. Recommendations for a nomenclature system for human gene mutations
2. 1999. Allele variant entry form (draft 4). Retrieved 17 July 2001 from www.genomic.unimelb.edu.au/mdi/entry.html.
3. Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities
4. Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locus
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