Detection of an Atypical 22q11 Deletion That Has No Overlap with the DiGeorge Syndrome Critical Region
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference17 articles.
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2. Conotruncal anomaly face syndrome is associated with the deletion within chromosome 22q11;Burn;J Med Genet,1993
3. A high resolution integrated yeast artificial chromosome clone map of human chromosome 22;Collins;Nature Suppl,1995
4. Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity;Demczuk;Hum Mol Genet,1995
5. syndrome: consistent deletions and microdeletions of 22q11;Driscoll;Am J Hum Genet,1992
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2. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia;American Journal of Medical Genetics Part A;2018-10
3. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype;Journal of Clinical Laboratory Analysis;2018-07-25
4. Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR;BMC Medical Genetics;2014-10-14
5. Decreased DGCR8 Expression and miRNA Dysregulation in Individuals with 22q11.2 Deletion Syndrome;PLoS ONE;2014-08-01
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