Segmental Duplications, Genomic
"Segmental Duplications, Genomic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Low-copy (2-50) repetitive DNA elements that are highly homologous and range in size from 1000 to 400,000 base pairs.
|Segmental Duplications, Genomic
- Segmental Duplications, Genomic
- Duplication, Genomic Segmental
- Duplications, Genomic Segmental
- Genomic Segmental Duplication
- Genomic Segmental Duplications
- Segmental Duplication, Genomic
- Segmental Duplications
- Duplication, Segmental
- Duplications, Segmental
- Segmental Duplication
- Low-Copy Repeats
- Low Copy Repeats
- Low-Copy Repeat
- Repeat, Low-Copy
- Repeats, Low-Copy
- Low-Copy Repeats, DNA
- DNA Low-Copy Repeat
- DNA Low-Copy Repeats
- Low Copy Repeats, DNA
- Low-Copy Repeat, DNA
- Repeat, DNA Low-Copy
- Repeats, DNA Low-Copy
- Low-Copy Repeat Sequences
- Low Copy Repeat Sequences
- Low-Copy Repeat Sequence
- Repeat Sequence, Low-Copy
- Repeat Sequences, Low-Copy
- Sequence, Low-Copy Repeat
- Sequences, Low-Copy Repeat
Below are MeSH descriptors whose meaning is more general than "Segmental Duplications, Genomic".
Below are MeSH descriptors whose meaning is more specific than "Segmental Duplications, Genomic".
This graph shows the total number of publications written about "Segmental Duplications, Genomic" by people in this website by year, and whether "Segmental Duplications, Genomic" was a major or minor topic of these publications.
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Below are the most recent publications written about "Segmental Duplications, Genomic" by people in Profiles.
Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing. BMC Genomics. 2017 Dec 19; 18(1):977.
LTR-mediated retroposition as a mechanism of RNA-based duplication in metazoans. Genome Res. 2016 12; 26(12):1663-1675.
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption. Am J Med Genet A. 2013 Jul; 161A(7):1523-30.
LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining. J Hum Genet. 2011 Jul; 56(7):516-23.