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...

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Detalhes bibliográficos

Publicado no:	Clin Diagn Lab Immunol
Principais autores:	Sullivan, Kathleen E., McDonald-McGinn, Donna, Driscoll, Deborah A., Emanuel, Beverly S., Zackai, Elaine H., Jawad, Abbas F.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 1999
Assuntos:	Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC95796/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10548584/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/cdli.6.6.906-911.1999
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