| Literature DB >> 29564815 |
Maki Fukami1, Hiroki Kurahashi2.
Abstract
Chromothripsis was initially described as a novel cause of chromosomal rearrangements in cancer cells and was subsequently implicated in the development of gross chromosomal rearrangements in the germline. Other catastrophic cellular events such as chromoanasynthesis and chromoplexy have also been observed in human cells. Such events have been associated with various phenotypes including mental retardation and congenital malformations. Here, we introduce representative cases of human disorders arising from somatic or germline chromothripsis or similar catastrophic events. In this chapter, we use the term "chromoanagenesis" to indicate all catastrophic events including chromothripsis.Entities:
Keywords: Congenital anomaly; Deletion; Duplication; Gene; Germline; Rearrangement; Tumor
Mesh:
Year: 2018 PMID: 29564815 DOI: 10.1007/978-1-4939-7780-2_2
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745