Citations for
1TBX3, UMS
TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome.
Kumar P P, Franklin S, Emechebe U, Hu H, Moore B, Lehman C, Yandell M, Moon AM.
PLoS Genet 10(3):e1004247. doi: 10.1371/journal.pgen.1004247. eCollection 2014 Mar. 2014
2TBX3, UMS
Ulnar Mammary syndrome and TBX3: expanding the phenotype.
Linden H, Williams R, King J, Blair E, Kini U.
Am J Med Genet A 149A(12):2809-12.PMID: 19938096 2009
3TBX3, UMS
Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.
Klopocki E, Neumann LM, Tonnies H, Ropers HH, Mundlos S, Ullmann R.
Eur J Hum Genet 14(12):1274-9. Epub 2006 Aug 9. 2006
4UMS, TBX3
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.
Bamshad M, et al.
Am J Hum Genet 64(6):1550-62. 1999
5TBX3, UMS
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome.
Bamshad M, Lin RC, Law DJ, Watkins WC, Krakowiak PA, Moore ME, Franceschini P, Lala R, Holmes LB, Gebuhr TC, Bruneau BG, Schinzel A, Seidman JG, Seidman CE, Jorde LB.
Nat Genet 16(3):311-5. 1997
6UMS
A gene for ulnar-mammary syndrome maps to 12q23-q24.1.
Bamshad M, Krakowiak PA, Watkins WS, Root S, Carey JC, Jorde LB.
Hum Mol Genet 4(10):1973-7. 1995