Hematological abnormalities and 22q11.2 deletion syndrome

The 22q11.2 deletion syndrome (22q11DS) is a common genetic disease characterized by broad phenotypic variability. Despite the small number of studies describing hematological alterations in individuals with 22q11DS, it appears that these abnormalities are more frequent than previously imagined. Thu...

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Detalhes bibliográficos
Main Authors: Rosa, Rafael Fabiano Machado, Rosa, Rosana Cardoso Manique, dos Santos, Pedro Paulo Albino, Zen, Paulo Ricardo Gazzola, Paskulin, Giorgio Adriano
Formato: Artigo
Idioma:Inglês
Publicado em: Associação Brasileira de Hematologia e Hemoterapia 2011
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3520641/
https://ncbi.nlm.nih.gov/pubmed/23284264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5581/1516-8484.20110037
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