Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: A new component manifestation of deletion 22q11?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference12 articles.
1. Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/Velo-cardio-facial chromosomal region in 22q11.2
2. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
3. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
4. Soluble FcϵR II levels in normal children and patients with immunodeficiency diseases
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2. Platelet parameters in children with chromosome 22q11 deletion and conotruncal heart defects;Congenital Heart Disease;2018-03-05
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