Kalaudjieva L.,1991a


Kalaydjieva L., Dworniczak B., Aulehla-Scholz C., Devoto M, Romeo G., Sturhmann M., Kucinskas V., Yurgelyavicius V., Horst J. Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria. - J.Med.Genet.,1991, v. 28, p. 686-690.