Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics,Molecular Biology
Cited by 90 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. Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases;American Journal of Medical Genetics Part A;2023-11-16
2. A De Novo sSMC (22) Characterized by High-Resolution Chromosome Microarray Analysis in a Chinese Boy with Cat-Eye Syndrome;Case Reports in Genetics;2021-02-27
3. Cecr2 mutant mice as a model for human cat eye syndrome;Scientific Reports;2021-02-04
4. Atypical presentation of Cat Eye Syndrome in an infant with Peters anomaly and microphthalmia with cyst;Ophthalmic Genetics;2020-08-31
5. Optic nerve coloboma as extension of the phenotype of 22q11.23 duplication syndrome: a case report;BMC Ophthalmology;2020-08-17
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