Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
Analysis of De Novo HOXA13 Polyalanine Expansions Supports Replication Slippage Without Repair in Their Generation.
Owens KM, Quinonez SC, Thomas PE, Keegan CE, Lefebvre N, Roulston D, Larsen CA, Stadler HS, Innis JW.
Am J Med Genet A. 2013 May;161(5):1019-27. doi: 10.1002/ajmg.a.35843. Epub 2013 Mar 26.
Related citations
Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.
Hosoki K, Ohta T, Fujita K, Nishigaki S, Shiomi M, Niikawa N, Saitoh S.
Pediatr Int. 2012 Jun;54(3):e22-5. doi: 10.1111/j.1442-200X.2011.03550.x. No abstract available.
Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster.
Fryssira H, Makrythanasis P, Kattamis A, Stokidis K, Menten B, Kosaki K, Willems P, Kanavakis E.
Mol Syndromol. 2011 Dec;2(1):45-49. Epub 2011 Nov 12.
Hallux valgus interphalangeus and a novel mutation in HOXA13. Part of the broadening spectrum of Hand-Foot-Genital syndrome.
Parker L, Mangwani J, Wakeling E, Singh D.
Foot Ankle Surg. 2011 Jun;17(2):e28-30. doi: 10.1016/j.fas.2010.12.003. Epub 2011 Jan 19.
Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster.
Jun KR, Seo EJ, Lee JO, Yoo HW, Park IS, Yoon HK.
Am J Med Genet A. 2011 Mar;155A(3):642-7. doi: 10.1002/ajmg.a.33860. Epub 2011 Feb 22.
A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
Fertil Steril. 2010 Sep;94(4):1235-8. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9.
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M, Reutter H, Innis JW.
Am J Med Genet A. 2007 Dec 15;143A(24):3161-8.
Abnormal urethra formation in mouse models of split-hand/split-foot malformation type 1 and type 4.
Suzuki K, Haraguchi R, Ogata T, Barbieri O, Alegria O, Vieux-Rochas M, Nakagata N, Ito M, Mills AA, Kurita T, Levi G, Yamada G.
Eur J Hum Genet. 2008 Jan;16(1):36-44. Epub 2007 Sep 19.
HOX genes: seductive science, mysterious mechanisms.
Lappin TR, Grier DG, Thompson A, Halliday HL.
Ulster Med J. 2006 Jan;75(1):23-31. Review. Erratum in: Ulster Med J. 2006 May;75(2):135.
Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?
Kosaki R, Higuchi M, Mitsui N, Matsushima K, Ohashi H, Kosaki K.
Congenit Anom (Kyoto). 2005 Mar;45(1):35-8.
The pathophysiology of HOX genes and their role in cancer.
Grier DG, Thompson A, Kwasniewska A, McGonigle GJ, Halliday HL, Lappin TR.
J Pathol. 2005 Jan;205(2):154-71. Review.
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model.
Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B.
Hum Mol Genet. 2004 Nov 15;13(22):2841-51. Epub 2004 Sep 22.
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.
Dunø M, Hove H, Kirchhoff M, Devriendt K, Schwartz M.
Hum Genet. 2004 Nov;115(6):459-67. Epub 2004 Sep 18.
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on