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Fox's in development and disease.
Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS. Lehmann OJ, et al. Among authors: sowden jc. Trends Genet. 2003 Jun;19(6):339-44. doi: 10.1016/S0168-9525(03)00111-2. Trends Genet. 2003. PMID: 12801727 Review.
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
Idrees F, Bloch-Zupan A, Free SL, Vaideanu D, Thompson PJ, Ashley P, Brice G, Rutland P, Bitner-Glindzicz M, Khaw PT, Fraser S, Sisodiya SM, Sowden JC. Idrees F, et al. Among authors: sowden jc. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):184-91. doi: 10.1002/ajmg.b.30237. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16389592
A review of anterior segment dysgeneses.
Idrees F, Vaideanu D, Fraser SG, Sowden JC, Khaw PT. Idrees F, et al. Among authors: sowden jc. Surv Ophthalmol. 2006 May-Jun;51(3):213-31. doi: 10.1016/j.survophthal.2006.02.006. Surv Ophthalmol. 2006. PMID: 16644364 Review.
122 results