Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference136 articles.
1. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features;Kitsiou-Tzeli;In Vivo,2004
2. Variable phenotypes in velocardiofacial syndrome with chromosomal deletion;Motzkin;J Pediatr,1993
3. Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients;Markert;Blood,2003
4. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci;Berend;Am J Med Genet,2000
5. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion;Bartsch;Am J Med Genet,2003
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