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Drosophila Model for the Analysis of Genesis of LIM-kinase 1-Dependent Williams-Beuren Syndrome Cognitive Phenotypes: INDELs, Transposable Elements of the Tc1/Mariner Superfamily and MicroRNAs

Genomic disorders, the syndromes with multiple manifestations, may occur sporadically due to unequal recombination in chromosomal regions with specific architecture. Therefore, each patient may carry an individual structural variant of DNA sequence (SV) with small insertions and deletions (INDELs) s...

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Podrobná bibliografie
Vydáno v:Front Genet
Hlavní autoři: Savvateeva-Popova, Elena V., Zhuravlev, Aleksandr V., Brázda, Václav, Zakharov, Gennady A., Kaminskaya, Alena N., Medvedeva, Anna V., Nikitina, Ekaterina A., Tokmatcheva, Elena V., Dolgaya, Julia F., Kulikova, Dina A., Zatsepina, Olga G., Funikov, Sergei Y., Ryazansky, Sergei S., Evgen‘ev, Michail B.
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2017
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5611441/
https://ncbi.nlm.nih.gov/pubmed/28979292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2017.00123
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