Mosaic deletion of 20pter due to rescue by somatic recombination
Author:
Affiliation:
1. Lineagen, Inc.; Salt Lake City Utah
2. Department of Pediatrics and Pathology; University of Utah; Salt Lake City Utah
3. ARUP Laboratories; Salt Lake City Utah
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37407/fullpdf
Reference20 articles.
1. Del(20p) with manifestations of arteriohepatic dysplasia;Byrne;Am J Med Genet,1986
2. Absence of heterozygosity due to template switching during replicative rearrangements;Carvalho;Am J Hum Genet,2015
3. Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients;Conlin;J Med Genet,2010a
4. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis;Conlin;Hum Mol Genet,2010b
5. Monosomy 20p due to a de novo del(20)(p12. 2). Clinical and radiological delineation of the syndrome;Garcia-Cruz;Ann Genet,1985
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