Cargando…
SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome
The DiGeorge/22q11-deletion syndrome (22q11DS), also known as velocardiofacial syndrome, is a congenital disease causing numerous structural and behavioral disorders, including cardiac outflow tract anomalies, craniofacial dysmorphogenesis, parathyroid and thymus hypoplasia, and mental disorders. It...
Autores principales: | Duband, Jean-Loup, Escot, Sophie, Fournier-Thibault, Claire |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961262/ https://www.ncbi.nlm.nih.gov/pubmed/27500073 http://dx.doi.org/10.1080/21675511.2016.1195050 |
Ejemplares similares
-
DiGeorge phenotype in the absence of 22q11 deletion – a case report
por: Taliana, N, et al.
Publicado: (2017) -
Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
por: Vergés, Laia, et al.
Publicado: (2014) -
Novel retinal observations in a child with DiGeorge (22q11.2 deletion) syndrome
por: Kozak, Igor, et al.
Publicado: (2022) -
Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management
por: Biggs, Sarah E., et al.
Publicado: (2023) -
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
por: Motahari, Zahra, et al.
Publicado: (2019)