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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. Traboulsi EI, et al. Among authors: finegold dn. Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2. Am J Ophthalmol. 2002. PMID: 12383817
Candidate gene analysis in primary lymphedema.
Ferrell RE, Kimak MA, Lawrence EC, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Lymphat Res Biol. 2008;6(2):69-76. doi: 10.1089/lrb.2007.1022. Lymphat Res Biol. 2008. PMID: 18564921
GJC2 missense mutations cause human lymphedema.
Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN. Ferrell RE, et al. Among authors: finegold dn. Am J Hum Genet. 2010 Jun 11;86(6):943-8. doi: 10.1016/j.ajhg.2010.04.010. Epub 2010 May 27. Am J Hum Genet. 2010. PMID: 20537300 Free PMC article.
Age of onset in hereditary lymphedema.
Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Levinson KL, et al. Among authors: finegold dn. J Pediatr. 2003 Jun;142(6):704-8. doi: 10.1067/mpd.2003.235. J Pediatr. 2003. PMID: 12838201
HGF and MET mutations in primary and secondary lymphedema.
Finegold DN, Schacht V, Kimak MA, Lawrence EC, Foeldi E, Karlsson JM, Baty CJ, Ferrell RE. Finegold DN, et al. Lymphat Res Biol. 2008;6(2):65-8. doi: 10.1089/lrb.2008.1524. Lymphat Res Biol. 2008. PMID: 18564920 Free PMC article.
106 results