权威例句
Creutzfeldt-Jakob Disease: Focus among Libyan Jews in IsraelLRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews.Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews.The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder populationMutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi JewsA mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.Struewing, J.P. et al. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N. Engl. J. Me...