Nadia Chuzhanova
0000-0002-4655-3618
56 papers found
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Long homopurine•homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region
At Least 1 in 20 16S rRNA Sequence Records Currently Held in Public Repositories Is Estimated To Contain Substantial Anomalies
Intrachromosomal serial replication slippage intransgives rise to diverse genomic rearrangements involving inversions
Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16
Complex gene rearrangements caused by serial replication slippage
Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations.
Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosome
Meta-analysis of gross insertions causing human genetic disease: novel mutational mechanisms and the role of replication slippage
Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes)
Breakpoints of gross deletions coincide with non-B DNA conformations
Genomic rearrangements in theCFTRgene: Extensive allelic heterogeneity and diverse mutational mechanisms
A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype
Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends
Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs
Meta-analysis of indels causing human genetic disease: Mechanisms of Mutagenesis and the Role of Local DNA Sequence Complexity
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