Биоинформатический анализ дупликации в участке 11p15.5 при расстройствах аутистического спектра с «реттоподобным фенотипом»
About the Authors
Кирилл ВасинRussian Federation
Ю. Юров
Russian Federation
С. Ворсанова
Russian Federation
И. Юров
Russian Federation
References
1. Vorsanova S.G., Iourov I.Y., Yurov Y.B. Neurological, genetic and epigenetic features of Rett syndrome. Journal of Pediatric Neurology. 2004;2(4):179-190. DOI:10.1055/s-0035-1557218
2. Iourov I.Y., Vorsanova S.G., Voinova V.Y., Kurinnaia O.S., Zelenova M.A., Demidova I.A., Yurov Y.B. Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease. Mol Cytogenet. 2013;6(1):53. DOI: 10.1186/1755-8166-6-53
3. Iourov I.Y., Vorsanova S.G., Yurov Y.B. In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for ba- sic and clinical genome research. Molecular Cytogenetics. 2014;7(1):98. DOI:10.1186/s13039-014-0098-z
Review
For citations:
, , , . Psychiatry (Moscow) (Psikhiatriya). 2016;(71):44-44а. (In Russ.)