First, the function of the ROBO2-SLIT2 pathway in patterning the kidney domain in the early urogenital ridge was examined. Loss of Robo2 in mouse and human is known to result in the formation of supernumerary kidneys driven by an expansion of Gdnf expression. Examination of the early urogenital ridge revealed that the number of cells in the nephrogenic cord was increased in Robo2-null mice, resulting in ectopic caudal mesonephric tubules and an expanded metanephric mesenchyme. In addition, the metanephric mesenchyme fails to separate from the Wolffian duct during kidney development, suggesting that the morphogenesis of the metanephric mesenchyme away from the Wolffian duct may result from active cell migration.Second, the anterior-posterior extension of the intermediate mesoderm and the upper and lower urinary tract differentiation was investigated in Wnt5a-null mice. It was observed that Wnt5a-null mice develop a horseshoe kidney. Underlying horseshoe kidney formation, Wolffian duct migration and insertion into the cloaca are disrupted in Wnt5a-null mice. These defects were reminiscent of mice with perturbed retinoic acid signalling, which led to the finding that the Wolffian duct is exposed to abnormally high levels of retinoic acid in Wnt5a-null mice. Therefore, the likely underlying cause of Wolffian duct migration defects in Wnt5a-null mice is exposure to increased retinoic acid concentrations, secondary to the failure of global axis extension. iv Third, the anterior-posterior extension of the gonad domain in intermediate mesoderm patterning was investigated by studying mouse mutants with a defect in retrograde trafficking of primary cilia.Mouse mutants of the primary cilium component Ift144, develop XY and XX gonads that are larger than wild-type. Investigation of the early patterning of the urogenital ridge found the anteriorposterior domain of the gonad was extended with a concomitant extension of the embryo trunk axis.Extension of the anterior-posterior gonad axis resulted in an increase in testis cord number, suggesting that the gonad domain is partitioned along the available space rather than partitioned a finite number of times. In addition, somitogenesis in the trunk of the embryo was disrupted, with somitogenesis in the tail proceeding correctly, suggesting that perturbed somite segmentation may be the cause of the increased trunk extension. Thus, analysis of Ift144 mouse mutants has suggested that the length of the trunk axis of the embryo is the main determinant of the gonad anteriorposterior domain and helped to clarify the paradigm of testis cord formation.Fourth, the expression, regulation and function of the microRNA miR-202 was examined in testis differentiation. miR-202-5p/3p was detected as being expressed specifically in the Sertoli cells, during XY gonad differentiation. Over-expression of pri-miR-202 in XX gonads did not perturb XX gonad differentiation, suggesting that pri-miR-202 does not directly antagonize the XX differentiation pathway. Furthermore, investigation of the pri...