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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Detalles Bibliográficos
Autores principales: Rosa, Rafael Fabiano Machado, Rosa, Rosana Cardoso Manique, dos Santos, Pedro Paulo Albino, Zen, Paulo Ricardo Gazzola, Paskulin, Giorgio Adriano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Hematologia e Hemoterapia 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520641/
https://www.ncbi.nlm.nih.gov/pubmed/23284264
http://dx.doi.org/10.5581/1516-8484.20110037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520641/
https://www.ncbi.nlm.nih.gov/pubmed/23284264
http://dx.doi.org/10.5581/1516-8484.20110037

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