Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Nadezda V. Shilova"'
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-10 (2021)
Abstract Copy number gain 17 p13.3p13.1 was detected by chromosomal microarray (CMA) in a girl with developmental/speech delay and facial dysmorphism. FISH studies made it possible to establish that the identified genomic imbalance is the unbalanced
Externí odkaz:
https://doaj.org/article/b20dabdd1d7e4dcda985e42f0302774e
Autor:
Darya A. Yurchenko, Marina E. Minzhenkova, Elena L. Dadali, Zhanna G. Markova, Galina E. Rudenskaya, Galina N. Matyushchenko, Ilya V. Kanivets, Nadezda V. Shilova
Publikováno v:
Biomedicines, Vol 10, Iss 3, p 567 (2022)
Inverted duplication syndrome with an adjacent terminal deletion of the short arm of chromosome 8—inv dup del(8p)—is a rare complex structural chromosomal rearrangement with a wide range of clinical manifestations. Molecular cytogenetic variants
Externí odkaz:
https://doaj.org/article/8d9a6b2c84534c6195f772851c460bdf
Autor:
Svetlana V Kostyuk, Marina S Konkova, Elizaveta S Ershova, Anna J Alekseeva, Tatiana D Smirnova, Sergey V Stukalov, Ekaterina A Kozhina, Nadezda V Shilova, Tatiana V Zolotukhina, Zhanna G Markova, Vera L Izhevskaya, Ancha Baranova, Natalia N Veiko
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e77469 (2013)
BACKGROUND:Cell free DNA (cfDNA) circulates throughout the bloodstream of both healthy people and patients with various diseases and acts upon the cells. Response to cfDNA depends on concentrations and levels of the damage within cfDNA. Oxidized extr
Externí odkaz:
https://doaj.org/article/cd4355125eab4851ba01f18f47eea8f0