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Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development

  • Kwon, Soon Sung (Department of Laboratory Medicine, Yonsei University College of Medicine) ;
  • Kim, Jieun (Department of Laboratory Medicine, Soon Chun Hyang University College of Medicine) ;
  • Shin, Saeam (Department of Laboratory Medicine, Hallym University College of Medicine) ;
  • Lee, Seung-Tae (Department of Laboratory Medicine, Yonsei University College of Medicine) ;
  • Lee, Kyung-A (Department of Laboratory Medicine, Yonsei University College of Medicine) ;
  • Choi, Jong Rak (Department of Laboratory Medicine, Yonsei University College of Medicine)
  • Received : 2017.02.01
  • Accepted : 2017.09.19
  • Published : 2018.01.01

Abstract

Keywords

References

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  2. Meloni Vde F, Piazzon FB, Soares Mde F, Takeno SS, Christofolini DM, Kulikowski LD, et al. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype. Gene 2012;496:59-62. https://doi.org/10.1016/j.gene.2012.01.007
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