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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...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Rafael Fabiano Machado Rosa, Rosana Cardoso Manique Rosa, Pedro Paulo Albino dos Santos, Paulo Ricardo Gazzola Zen, Giorgio Adriano Paskulin
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2011-01-01
Schriftenreihe:Revista Brasileira de Hematologia e Hemoterapia
Schlagworte:
Blood platelets
Thrombocytopenia
Bernard-Soulier syndrome
DiGeorge syndrome
In situ hybridization
Chromosomes, Human, Pair 22
Online-Zugang:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842011000200015
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