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...
Main Authors: | Rafael Fabiano Machado Rosa, Rosana Cardoso Manique Rosa, Pedro Paulo Albino dos Santos, Paulo Ricardo Gazzola Zen, Giorgio Adriano Paskulin |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2011-01-01
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Series: | Revista Brasileira de Hematologia e Hemoterapia |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842011000200015 |
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