Ocular findings associated with chromosome 22q11.2 duplication
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis;Shaikh;Hum Mol Genet,2000
2. The Philadelphia story: the 22q11.2 deletion: report on 250 patients;McDonald-McGinn;Genet Couns,1999
3. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9,500 pregnancies;Grati;Prenat Diagn,2015
4. Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients;Ensenauer;Am J Hum Genet,2003
5. 22q11. 2 duplication and congenital heart defects;Rosa;Arq Bras Cardiol,2009
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