Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis

A subset of neurofibromatosis type 1 patients develop tibial dysplasia, which can lead to pseudarthrosis. The tissue from the tibial pseudarthrosis region commonly has a somatic second hit in NF1: single-nucleotide variants, small deletions, or loss of heterozygosity (LOH). We used exome next-genera...

Full description

Saved in:
Bibliographic Details
Published in:J Mol Diagn
Main Authors: Margraf, Rebecca L., VanSant-Webb, Chad, Sant, David, Carey, John, Hanson, Heather, D'Astous, Jacques, Viskochil, Dave, Stevenson, David A., Mao, Rong
Format: Artigo
Language:Inglês
Published: American Society for Investigative Pathology 2017
Subjects:
Regular Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5417040/
https://ncbi.nlm.nih.gov/pubmed/28433079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmoldx.2017.01.008
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items