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Items: 5

1.

Gene Conversion-Like Events in the Diversification of Human Rearranged IGHV3-23*01 Gene Sequences.

Duvvuri B, Wu GE.

Front Immunol. 2012 Jun 15;3:158. doi: 10.3389/fimmu.2012.00158. eCollection 2012.

2.

Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencing.

Rossetti S, Hopp K, Sikkink RA, Sundsbak JL, Lee YK, Kubly V, Eckloff BW, Ward CJ, Winearls CG, Torres VE, Harris PC.

J Am Soc Nephrol. 2012 May;23(5):915-33. doi: 10.1681/ASN.2011101032. Epub 2012 Mar 1.

3.

Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency.

Coeli FB, Soardi FC, Bernardi RD, de Araújo M, Paulino LC, Lau IF, Petroli RJ, de Lemos-Marini SH, Baptista MT, Guerra-Júnior G, de-Mello MP.

BMC Med Genet. 2010 Jun 29;11:104. doi: 10.1186/1471-2350-11-104.

4.

Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair.

Chuzhanova N, Chen JM, Bacolla A, Patrinos GP, Férec C, Wells RD, Cooper DN.

Hum Mutat. 2009 Aug;30(8):1189-98. doi: 10.1002/humu.21020.

5.

Sequence features of HLA-DRB1 locus define putative basis for gene conversion and point mutations.

von Salomé J, Kukkonen JP.

BMC Genomics. 2008 May 19;9:228. doi: 10.1186/1471-2164-9-228.

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