mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing
PDF) Characterization of a Mutation in the Lens-Specific CP49 in
DNA sequence flanking the 6-kb deletion. Uppercase letter: sequence
DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development: Cell
Life, Free Full-Text
Widespread divergent transcription from bacterial and archaeal promoters is a consequence of DNA-sequence symmetry
Linkage Disequilibrium between Two High-Frequency Deletion Polymorphisms: Implications for Association Studies Involving the glutathione-S transferase (GST) Genes
Modulation of DNA End Joining by Nuclear Proteins - ScienceDirect
Teri Seeberger's research works University of Washington Seattle
Helper-independent and AAV-ITR-independent chromosomal integration of double-stranded linear DNA vectors in mice: Molecular Therapy
PDF) Characterization of a Mutation in the Lens-Specific CP49 in
Frontiers Cataloging Human PRDM9 Allelic Variation Using Long-Read Sequencing Reveals PRDM9 Population Specificity and Two Distinct Groupings of Related Alleles
DNA sequence flanking the 6-kb deletion. Uppercase letter: sequence