Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Cited by 23 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. Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region;International Journal of Molecular Sciences;2022-03-20
2. Trisomy Xp and partial tetrasomy Xq resulting from gain of a rearranged X chromosome in a female fetus: pathogenic or not?;Molecular Cytogenetics;2015-07-25
3. Terminal 18q deletions are stabilized by neotelomeres;Molecular Cytogenetics;2015-05-13
4. Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3;Human Molecular Genetics;2015-04-23
5. Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype;Gene;2012-09
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