The mouse Ulnaless mutation deregulates posterior HoxD gene expression and alters appendicular patterning

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				G. Caronia, F. R. Goodman, C. M. E. McKeown, P. J. Scambler, and V. Zappavigna An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function Development, April 15, 2003; 130(8): 1701 - 1712. [Abstract] [Full Text] [PDF]

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				H Sugawara, M Egashira, N Harada, T C Jakobs, K Yoshiura, T Kishino, T Ohta, N Niikawa, and N Matsumoto Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasia J. Med. Genet., July 1, 2002; 39(7): e34 - 34. [Full Text] [PDF]

				Y. Zhao and S. S. Potter Functional specificity of the Hoxa13 homeobox Development, August 15, 2001; 128(16): 3197 - 3207. [Abstract] [Full Text] [PDF]

				M. Kmita, F. van der Hoeven, J. Zákány, R. Krumlauf, and D. Duboule Mechanisms of Hox gene colinearity: transposition of the anterior Hoxb1 gene into the posterior HoxD complex Genes & Dev., January 15, 2000; 14(2): 198 - 211. [Abstract] [Full Text]

				A Zuniga and R Zeller Gli3 (Xt) and formin (ld) participate in the positioning of the polarising region and control of posterior limb-bud identity Development, January 1, 1999; 126(1): 13 - 21. [Abstract] [PDF]

				Y Herault, J Beckers, T Kondo, N Fraudeau, and D Duboule Genetic analysis of a Hoxd-12 regulatory element reveals global versus local modes of controls in the HoxD complex Development, January 5, 1998; 125(9): 1669 - 1677. [Abstract] [PDF]

				Y Herault, N Fraudeau, J Zakany, and D Duboule Ulnaless (Ul), a regulatory mutation inducing both loss-of-function and gain-of-function of posterior Hoxd genes Development, January 9, 1997; 124(18): 3493 - 3500. [Abstract] [PDF]