Longitudinal Analysis of Lymphocyte Function and Numbers in the First Year of Life in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Chromosome 22q11.2 deletion syndrome is a common syndrome typically consisting of variable cardiac defects, hypoparathyroidism, developmental delay, and immunodeficiency. The hemizygous deletion has variable effects on the immune system even within the same kindred, and the extent of the immunodefic...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Sullivan, Kathleen E., McDonald-McGinn, Donna, Driscoll, Deborah A., Emanuel, Beverly S., Zackai, Elaine H., Jawad, Abbas F.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Microbiology 1999
Materias:
Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC95796/
https://ncbi.nlm.nih.gov/pubmed/10548584
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares