Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

Author:

Barber J. C. K.,Reed Caroline J.,Joyce Christine A.,Dahoun S. P

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Cited by 42 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. Cytogenetic Analysis;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2019

2. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16;Taiwanese Journal of Obstetrics and Gynecology;2017-08

3. Euchromatic Variants;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

4. References;Benign & Pathological Chromosomal Imbalances;2014

5. Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2;European Journal of Human Genetics;2013-09-18

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