Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics
Author:
Publisher
Spandidos Publications
Subject
Genetics,General Medicine
Cited by 18 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. Clinical characteristics and laboratory diagnosis of Pallister-Killian syndrome;2024-06-10
2. A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature;Frontiers in Genetics;2024-02-23
3. Small supernumerary marker chromosomes in prenatal diagnosis—molecular characterization and clinical outcomes;Frontiers in Genetics;2024-01-08
4. Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers;Bulletin of Russian State Medical University;2024-01
5. Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome;Frontiers in Genetics;2022-09-26
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