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Low copy repeats
(Lcrs) in 22Q11 Mediate Deletions, Duplications, Translocations, and Genomic Instability: an Update and Literature Review Tamim H
Copy Number Variation and Huntington's Disease
Gentles Et Al 2007 Gen Res.Pdf
Repetitive Elements in Humans
Recent Advance in Our Understanding of the Molecular Nature of Chromosomal Abnormalities
Human Genetics Lecture #1 March 25, 2014
Novel Methods to Study Genomic Fragility and Structural Variation
The 22Q11 Low Copy Repeats Are Characterized by Unprecedented Size and Structural Variability
Non-Hotspot-Related Breakpoints of Common Deletions In
Disorders of the Genome Architecture: a Review
Structural Features of the Genome Can Lead to DNA Rearrangements And
An Overview of Duplicated Gene Detection Methods: Why the Duplication Mechanism Has to Be Accounted for in Their Choice
Recombination Hot Spots and Human Disease Smita M
Diverse Mutational Mechanisms Cause Pathogenic Subtelomeric Rearrangements
Recurrent Rearrangements in the Proximal 15Q11–Q14 Region: a New Breakpoint Cluster Specific to Unbalanced Translocations
A Novel Third Type of Recurrent NF1 Microdeletion Mediated by Non
(Cnvs) with CRISPR-CATCH/LONG-READ SEQUENCING Bo Zhou1, Giwon Shin2, Lisanne Vervoort3, Stephanie U
Repetitive Sequences in Complex Genomes: Structure and Evolution
Top View
The 22Q11 Low Copy Repeats Are Characterized by Unprecedented Size and Structure Variability
What We Can Learn from Structural Variation at Human Chromosome Band 8P23.1
Structure of Chromosomal Duplicons and Their Role in Mediating Human Genomic Disorders
Interspersed Repeats and Other Mementos of Transposable Elements in Mammalian Genomes Arian FA Smit
A Model of Segmental Duplication Formation in Drosophila Melanogaster
Complete and Haplotype-Specific Sequence Assembly of Segmental Duplication
Superior Ab Initio Identification, Annotation and Characterisation of Tes and Segmental Duplications from Genome Assemblies
Extreme Enrichment of VNTR-Associated Polymorphicity In
21 Monosomy 1P36 As a Model for the Molecular Basis of Terminal Deletions
4 Ancient Transposable Elements, Processed Pseudogenes, and Endogenous Retroviruses
Consequences of 22Q11.2 Microdeletion on the Genome, Individual and Population Levels
Integrated Small Copy Number Variations and Epigenome Maps of Disorders of Sex Development
Transposable Elements Are a Significant Contributor to Tandem
Origin-Dependent Inverted-Repeat Amplification: a Replication-Based Model for Generating Palindromic Amplicons
Low Copy Repeat on Chromosome 16A Has Driven Genome Evolution and Created a New Gene Family in Primates and Humans
Inverted Duplications Deletions: Underdiagnosed Rearrangements??
Duplication and Relocation of the Functional DPY19L2 Gene Within Low Copy Repeats Andrew R Carson1,2, Joseph Cheung1 and Stephen W Scherer*1,2
Development of a CRISPR- Mediated Gene Editing Approach for the Treatment of Pathogenic Duplications