Novel retinal observations in a child with DiGeorge (22q11.2 deletion) syndrome
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference10 articles.
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2. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome;Koczkowska;J Appl Genet,2017
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4. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet,1997
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Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The Co-Occurrence of 22q11.2 Deletion Syndrome and Epithelial Basement Membrane Dystrophy: A Case Report and Review of the Literature;Life;2024-08-13
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