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24. Lymphedema-distichiasis syndrome and FOXC2 gene mutation. Traboulsi EI; Al-Khayer K; Matsumoto M; Kimak MA; Crowe S; Wilson SE; Finegold DN; Ferrell RE; Meisler DM Am J Ophthalmol; 2002 Oct; 134(4):592-6. PubMed ID: 12383817 [TBL] [Abstract][Full Text] [Related]
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31. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Brice G; Mansour S; Bell R; Collin JR; Child AH; Brady AF; Sarfarazi M; Burnand KG; Jeffery S; Mortimer P; Murday VA J Med Genet; 2002 Jul; 39(7):478-83. PubMed ID: 12114478 [TBL] [Abstract][Full Text] [Related]
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34. Distichiasis-lymphedema syndrome: tetralogy of Fallot, chylothorax, and neonatal death. Chen E; Larabell SK; Daniels JM; Goldstein S Am J Med Genet; 1996 Dec; 66(3):273-5. PubMed ID: 8985486 [TBL] [Abstract][Full Text] [Related]
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