Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome

22q11.2 deletion syndrome (22q11.2DS) is the most common genomic disorder with an extremely broad phenotypic spectrum. The aim of our study was to investigate how often the additional variants in the genome can affect clinical variation among patients with the recurrent deletion. To examine the pres...

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Detalles Bibliográficos
Autores principales: Smyk, Marta, Geremek, Maciej, Ziemkiewicz, Kamila, Gambin, Tomasz, Kutkowska-Kaźmierczak, Anna, Kowalczyk, Katarzyna, Plaskota, Izabela, Wiśniowiecka-Kowalnik, Barbara, Bartnik-Głaska, Magdalena, Niemiec, Magdalena, Grad, Dominika, Piotrowicz, Małgorzata, Gieruszczak-Białek, Dorota, Pietrzyk, Aleksandra, Crowley, T. Blaine, Giunta, Victoria, McGinn, Daniel E., Zackai, Elaine H., Tran, Oanh, Emanuel, Beverly S., McDonald-McGinn, Donna M., Nowakowska, Beata A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048180/
https://www.ncbi.nlm.nih.gov/pubmed/36980952
http://dx.doi.org/10.3390/genes14030680

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048180/
https://www.ncbi.nlm.nih.gov/pubmed/36980952
http://dx.doi.org/10.3390/genes14030680

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