Genomic context of paralogous recombination hotspots mediating recurrentNF1 region microdeletion
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Reference62 articles.
1. Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination
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1. Atypical NF1 Microdeletions: Challenges and Opportunities for Genotype/Phenotype Correlations in Patients with Large NF1 Deletions;Genes;2021-10-19
2. Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletions;Human Genetics;2021-09-18
3. Ultra-deep amplicon sequencing indicates absence of low-grade mosaicism with normal cells in patients with type-1 NF1 deletions;Human Genetics;2018-11-26
4. Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences;Human Genetics;2018-07
5. Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletions;Human Genetics;2018-05
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