Human inversions and their functional consequences.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 369, doi. 10.1093/bfgp/elv020
- By:
- Publication type:
- Article
Works matching IS 20412649 AND DT 2015 AND VI 14 AND IP 5
Results: 8
1
2
Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 315, doi. 10.1093/bfgp/elv018
- By:
- Publication type:
- Article
3
Structural variants, much ado about nothing?
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 303, doi. 10.1093/bfgp/elv031
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- Publication type:
- Article
4
Complex and multi-allelic copy number variation in human disease.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 329, doi. 10.1093/bfgp/elv028
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- Publication type:
- Article
5
Adaptive potential of genomic structural variation in human and mammalian evolution.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 258, doi. 10.1093/bfgp/elv019
- By:
- Publication type:
- Article
6
The impact of human copy number variation on gene expression.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 352, doi. 10.1093/bfgp/elv017
- By:
- Publication type:
- Article
7
A decade of structural variants: description, history and methods to detect structural variation.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 305, doi. 10.1093/bfgp/elv014
- By:
- Publication type:
- Article
8
Somatic structural variation and cancer.
- Published in:
- Briefings in Functional Genomics, 2015, v. 14, n. 5, p. 339, doi. 10.1093/bfgp/elv016
- By:
- Publication type:
- Article