Format
Sort by

Send to

Choose Destination

Search results

Items: 3

1.

TBX6 null variants and a common hypomorphic allele in congenital scoliosis.

Wu N, Ming X, Xiao J, Wu Z, Chen X, Shinawi M, Shen Y, Yu G, Liu J, Xie H, Gucev ZS, Liu S, Yang N, Al-Kateb H, Chen J, Zhang J, Hauser N, Zhang T, Tasic V, Liu P, Su X, Pan X, Liu C, Wang L, Shen J, Shen J, Chen Y, Zhang T, Zhang J, Choy KW, Wang J, Wang Q, Li S, Zhou W, Guo J, Wang Y, Zhang C, Zhao H, An Y, Zhao Y, Wang J, Liu Z, Zuo Y, Tian Y, Weng X, Sutton VR, Wang H, Ming Y, Kulkarni S, Zhong TP, Giampietro PF, Dunwoodie SL, Cheung SW, Zhang X, Jin L, Lupski JR, Qiu G, Zhang F.

N Engl J Med. 2015 Jan 22;372(4):341-50. doi: 10.1056/NEJMoa1406829. Epub 2015 Jan 7.

2.

oriC region and replication termination site, dif, of the Xanthomonas campestris pv. campestris 17 chromosome.

Yen MR, Lin NT, Hung CH, Choy KT, Weng SF, Tseng YH.

Appl Environ Microbiol. 2002 Jun;68(6):2924-33.

3.

Chromosome map of Xanthomonas campestris pv. campestris 17 with locations of genes involved in xanthan gum synthesis and yellow pigmentation.

Tseng YH, Choy KT, Hung CH, Lin NT, Liu JY, Lou CH, Yang BY, Wen FS, Weng SF, Wu JR.

J Bacteriol. 1999 Jan;181(1):117-25.

Supplemental Content

Loading ...
Support Center