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Results: 7

Related Articles by Review for PubMed (Select 20506139)

1.

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

Szafranski P, Schaaf CP, Person RE, Gibson IB, Xia Z, Mahadevan S, Wiszniewska J, Bacino CA, Lalani S, Potocki L, Kang SH, Patel A, Cheung SW, Probst FJ, Graham BH, Shinawi M, Beaudet AL, Stankiewicz P.

Hum Mutat. 2010 Jul;31(7):840-50. doi: 10.1002/humu.21284.

2.

[New chromosomal syndromes].

Schluth-Bolard C, Till M, Edery P, Sanlaville D.

Pathol Biol (Paris). 2008 Sep;56(6):380-7. doi: 10.1016/j.patbio.2008.03.006. Epub 2008 May 7. Review. French.

PMID:
18467039
3.

Genomic and clinical characteristics of microduplications in chromosome 17.

Shchelochkov OA, Cheung SW, Lupski JR.

Am J Med Genet A. 2010 May;152A(5):1101-10. doi: 10.1002/ajmg.a.33248. Review.

PMID:
20425816
4.

Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversion.

Maurin ML, Labrune P, Brisset S, Le Lorc'h M, Pineau D, Castel C, Romana S, Tachdjian G.

Am J Med Genet A. 2009 Feb;149A(2):226-31. doi: 10.1002/ajmg.a.32603. Review.

PMID:
19161154
5.

The human clinical phenotypes of altered CHRNA7 copy number.

Gillentine MA, Schaaf CP.

Biochem Pharmacol. 2015 Jun 18. pii: S0006-2952(15)00328-7. doi: 10.1016/j.bcp.2015.06.012. [Epub ahead of print] Review.

PMID:
26095975
6.

The genetics of microdeletion and microduplication syndromes: an update.

Watson CT, Marques-Bonet T, Sharp AJ, Mefford HC.

Annu Rev Genomics Hum Genet. 2014;15:215-44. doi: 10.1146/annurev-genom-091212-153408. Epub 2014 Apr 16. Review.

7.

The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function.

Sinkus ML, Graw S, Freedman R, Ross RG, Lester HA, Leonard S.

Neuropharmacology. 2015 Sep;96(Pt B):274-88. doi: 10.1016/j.neuropharm.2015.02.006. Epub 2015 Feb 19. Review.

PMID:
25701707
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