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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Hlavní autoři: Rosa, Rafael Fabiano Machado, Rosa, Rosana Cardoso Manique, dos Santos, Pedro Paulo Albino, Zen, Paulo Ricardo Gazzola, Paskulin, Giorgio Adriano
Médium: Artigo
Jazyk:Inglês
Vydáno: Associação Brasileira de Hematologia e Hemoterapia 2011
Témata:
Case Report
On-line přístup: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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