Ophthalmic abnormalities in Wieacker-Wolff syndrome
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology and Child Health
Reference11 articles.
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4. A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia;Wieacker;Am J Med Genet,1985
5. ZC4H2 deletions can cause severe phenotype in female carriers;Zanzottera;Am J Med Genet Part A,2017
Cited by 3 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. Genotype-Phenotype Correlations and Sex Differences in ZC4H2-Associated Rare Disorder;Pediatric Neurology;2024-09
2. Clinical case of Wieacker–Wolff syndrome in a 5-year girl;L.O. Badalyan Neurological Journal;2023-08-30
3. Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene;Ophthalmic Genetics;2023-07-31
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