Candidate modifier genes for immune function in 22q11.2 deletion syndrome

BACKGROUND: The 22q11.2 deletion syndrome (22q11.2DS) is the most common contiguous microdeletion affecting humans and exhibits extreme phenotypic heterogeneity. Patients can manifest any combination of comorbidities including congenital heart disease, hypoparathyroidism, cleft palate, kidney abnorm...

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Detalles Bibliográficos
Autores principales: Pinnaro, Catherina T., Henry, Travis, Major, Heather J., Parida, Mrutyunjaya, DesJardin, Lucy E., Manak, John R., Darbro, Benjamin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978229/
https://www.ncbi.nlm.nih.gov/pubmed/31830774
http://dx.doi.org/10.1002/mgg3.1057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978229/
https://www.ncbi.nlm.nih.gov/pubmed/31830774
http://dx.doi.org/10.1002/mgg3.1057

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