 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.
| Descriptor ID |
D056916
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| MeSH Number(s) |
G02.111.570.080.708.565 G05.360.080.708.565
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| Concept/Terms |
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 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
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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 UAMS Profiles 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 over the past ten years.
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Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, Pontillo M, Armando M, Di Fabio F, Vicari S, van den Bree M, Moss H, Owen MJ, Murphy KC, Murphy CM, Murphy D, Schoch K, Shashi V, Tassone F, Simon TJ, Shprintzen RJ, Campbell L, Philip N, Heine-Su?er D, Garc?a-Mi?a?r S, Fern?ndez L, Bearden CE, Vingerhoets C, van Amelsvoort T, Eliez S, Schneider M, Vorstman JAS, Gothelf D, Zackai E, Agopian AJ, Gur RE, Bassett AS, Emanuel BS, Goldmuntz E, Mitchell LE, Wang T, Morrow BE. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. Am J Hum Genet. 2020 01 02; 106(1):26-40.
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