An Interstitial 20q11.21 Microdeletion Causing Mild Intellectual Disability and Facial Dysmorphisms

por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Yurov, Yuri B.
Publicado 2013

An Interstitial Deletion at 10q26.2q26.3

por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Yurov, Yuri B.
Publicado 2014

Somatic mosaicism in the diseased brain

por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Kutsev, Sergei I., Yurov, Yuri B.
Publicado 2022

Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

por Iourov, Ivan Y, Vorsanova, Svetlana G, Kurinnaia, Oxana S, Zelenova, Maria A, Silvanovich, Alexandra P, Yurov, Yuri B
Publicado 2012

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

por Iourov, Ivan Y., Vorsanova, Svetlana G., Yurov, Yuri B., Zelenova, Maria A., Kurinnaia, Oxana S., Vasin, Kirill S., Kutsev, Sergei I.
Publicado 2020

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

por Iourov, Ivan Y, Vorsanova, Svetlana G, Voinova, Victoria Y, Kurinnaia, Oxana S, Zelenova, Maria A, Demidova, Irina A, Yurov, Yuri B
Publicado 2013