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pro vyhledávání: '"Bombardirova TD"'
Autor:
Kozlova IuO, N.P. Kotlukova, Simonova Lv, T.V. Zolotukhina, Kazanceva Ia, Poliakov Av, V. G. Antonenko, Bombardirova Td, M.E. Minzhenkova, N. V. Shilova, V. V. Zabnenkova, Levchenko Eg
Publikováno v:
Russian Journal of Genetics. 50:528-535
In a group of 140 patients with typical phenotype, the 22q11.2 microdeletion was detected in 43 patients (32%) using FISH and MLPA methods. There were no deletions of other chromosomal loci causing to phenotypes similar to the 22q11.2 deletion syndro