Zobrazeno 1 - 2
of 2
pro vyhledávání: '"V. M. Sivokha"'
Autor:
V. M. Sivokha, M.E. Lopatkina, S. A. Vasiliev, I. N. Lebedev, O. Y. Vasilieva, N.A. Skryabin, Elena O. Belyaeva, R. R. Savchenko, Lyudmila P. Nazarenko, D. I. Zhigalina
Publikováno v:
Russian Journal of Genetics. 56:739-746
Detection of translocations in subtelomeric regions of chromosomes is a serious diagnostic problem, because they are difficult to determine by conventional cytogenetics with G banding. The aim of this work was the development of the technology of DNA
Autor:
T V, Bushueva, L M, Kuzenkova, T É, Borovik, L P, Nazarenko, G N, Seitova, M N, Filimonova, N A, Pichkur, N V, Samonenko, T A, Shkurko, É N, Akhmadeeva, A K, Mardanova, É R, Garifullina, O P, Kovtun, Iu L, Bazhenova, I L, Alimova, E A, Kostiakova, L I, Minaĭcheva, O A, Saliukova, V M, Sivokha, O L, Rozenson
Publikováno v:
Annals of the Russian academy of medical sciences. 69:69-77
Background : Phenylketonuria (PKU) is an autosomal recessive inherited disease associated with impaired metabolism of the amino acids phenylalanine (Phe) and tyrosine. The main criterion for diagnosis of PKU is high blood Phe level determined during