Author:
Sebastio G,de Franchis R,Strisciuglio P,Andria G,Dionisi Vici C,Sabetta G,Gatti R,Cross N C,Cox T M
Subject
Genetics(clinical),Genetics
Reference5 articles.
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2. Catalytic deficiency of human aldolase B hereditary fructose intolerance caused by a common missense mutation;Cross, N.C.P.; Tolan, D.R.; Cox, T.M.;Cel,1988
3. Molecular analysis of aldolase B genes in hereditary fructose intolerance;Cross, N.C.P.; de Franchis, R.; Sebastio, G.;Lancet,1990
4. A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia;Cross, N.C.P.; Stoianov, L.M.; Cox, T.M.;Nucleic Acids Res,1990
5. Enzymatic amplification of 0-globin sequences and restriction site analysis for diagnosis of sickle cell anaemia;Saiki, R.K.; Scharf, S.; Faloona, F.;Science,1985
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