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Results: 14

Related Articles by Review for PubMed (Select 15273396)

1.

Large-scale copy number polymorphism in the human genome.

Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Månér S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, Reiner A, Gilliam TC, Trask B, Patterson N, Zetterberg A, Wigler M.

Science. 2004 Jul 23;305(5683):525-8.

2.

Copy-number polymorphisms: mining the tip of an iceberg.

Buckley PG, Mantripragada KK, Piotrowski A, Diaz de Ståhl T, Dumanski JP.

Trends Genet. 2005 Jun;21(6):315-7. Review.

PMID:
15922827
3.

[Structural variation in the human genome contributes to variation of traits].

Barøy T, Misceo D, Frengen E.

Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1951-5. Review. Norwegian.

4.
5.

Human genome variation in health and in neuropsychiatric disorders.

Buretić-Tomljanović A, Tomljanović D.

Psychiatr Danub. 2009 Dec;21(4):562-9. Review.

6.

Genomic copy number variation, human health, and disease.

Wain LV, Armour JA, Tobin MD.

Lancet. 2009 Jul 25;374(9686):340-50. doi: 10.1016/S0140-6736(09)60249-X. Epub 2009 Jun 15. Review.

PMID:
19535135
7.

Gene copy-number polymorphism in nature.

Schrider DR, Hahn MW.

Proc Biol Sci. 2010 Nov 7;277(1698):3213-21. doi: 10.1098/rspb.2010.1180. Epub 2010 Jun 30. Review.

8.

Gene duplication: a drive for phenotypic diversity and cause of human disease.

Conrad B, Antonarakis SE.

Annu Rev Genomics Hum Genet. 2007;8:17-35. Review.

PMID:
17386002
9.

The evolving picture of microdeletion/microduplication syndromes in the age of microarray analysis: variable expressivity and genomic complexity.

Deak KL, Horn SR, Rehder CW.

Clin Lab Med. 2011 Dec;31(4):543-64, viii. doi: 10.1016/j.cll.2011.08.008. Epub 2011 Oct 20. Review.

PMID:
22118736
10.

Copy-number variation: the end of the human genome?

Dear PH.

Trends Biotechnol. 2009 Aug;27(8):448-54. doi: 10.1016/j.tibtech.2009.05.003. Epub 2009 Jul 1. Review.

PMID:
19576644
11.

Idiopathic learning disability and genome imbalance.

Knight SJ, Regan R.

Cytogenet Genome Res. 2006;115(3-4):215-24. Review.

PMID:
17124403
12.

[Disease susceptibility genes and genome structural abnormalities associated with developmental disabilities].

Yamamoto T.

No To Hattatsu. 2014 Mar;46(2):131-5. Review. Japanese. No abstract available.

PMID:
24738191
13.

[Copy number variation: to recognize human birth defects from a new point of view].

Ma XJ, Huang GY.

Zhonghua Er Ke Za Zhi. 2010 Mar;48(3):232-5. Review. Chinese. No abstract available.

PMID:
20426964
14.

[Rare is frequent].

Jordan B.

Med Sci (Paris). 2012 Oct;28(10):893-6. doi: 10.1051/medsci/20122810020. Epub 2012 Oct 12. Review. French. No abstract available.

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