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Items: 9

1.

Identical repeated backbone of the human genome.

Zepeda-Mendoza CJ, Lemus T, Yáñez O, García D, Valle-García D, Meza-Sosa KF, Gutiérrez-Arcelus M, Márquez-Ortiz Y, Domínguez-Vidaña R, Gonzaga-Jauregui C, Flores M, Palacios R.

BMC Genomics. 2010 Jan 23;11:60. doi: 10.1186/1471-2164-11-60.

3.

The genomic basis of disease, mechanisms and assays for genomic disorders.

Stankiewicz P, Lupski JR.

Genome Dyn. 2006;1:1-16. doi: 10.1159/000092496. Review.

PMID:
18724050
4.

Detection and interpretation of genomic structural variation in mammals.

Hall IM, Quinlan AR.

Methods Mol Biol. 2012;838:225-48. doi: 10.1007/978-1-61779-507-7_11. Review.

PMID:
22228015
5.

Simple repetitive sequences in the genome: structure and functional significance.

Brahmachari SK, Meera G, Sarkar PS, Balagurumoorthy P, Tripathi J, Raghavan S, Shaligram U, Pataskar S.

Electrophoresis. 1995 Sep;16(9):1705-14. Review.

PMID:
8582360
6.

Child development and structural variation in the human genome.

Zhang Y, Haraksingh R, Grubert F, Abyzov A, Gerstein M, Weissman S, Urban AE.

Child Dev. 2013 Jan-Feb;84(1):34-48. doi: 10.1111/cdev.12051. Epub 2013 Jan 13. Review.

PMID:
23311762
7.

CNVs of noncoding cis-regulatory elements in human disease.

Spielmann M, Klopocki E.

Curr Opin Genet Dev. 2013 Jun;23(3):249-56. doi: 10.1016/j.gde.2013.02.013. Epub 2013 Apr 16. Review.

PMID:
23601627
8.

Major influence of repetitive elements on disease-associated copy number variants (CNVs).

Cardoso AR, Oliveira M, Amorim A, Azevedo L.

Hum Genomics. 2016 Sep 23;10(1):30. Review.

9.

Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA.

George CM, Alani E.

Crit Rev Biochem Mol Biol. 2012 May-Jun;47(3):297-313. doi: 10.3109/10409238.2012.675644. Epub 2012 Apr 12. Review.

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