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Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype

Lookup NU author(s): Dr Aneta MikulasovaORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Publication metadata

Author(s): Smetana J, Vallova V, Wayhelova M, Hladilkova E, Filkova H, Horinova V, Broz P, Mikulasova A, Gaillyova R, Kuglik P

Publication type: Article

Publication status: Published

Journal: Frontiers in Genetics

Year: 2021

Volume: 12

Online publication date: 29/10/2021

Acceptance date: 27/09/2021

Date deposited: 03/03/2022

ISSN (electronic): 1664-8021

Publisher: Frontiers Media SA

URL: https://doi.org/10.3389/fgene.2021.750110

DOI: 10.3389/fgene.2021.750110

PubMed id: 34777475


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Funding

Funder referenceFunder name
NU20-07-00145

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