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Milroy disease and the VEGFR-3 mutation phenotype.
Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand K, Sarfarazi M, Jeffery S, Mortimer P. Brice G, et al. Among authors: mortimer p. J Med Genet. 2005 Feb;42(2):98-102. doi: 10.1136/jmg.2004.024802. J Med Genet. 2005. PMID: 15689446 Free PMC article. Review.
Managing lymphoedema.
Mortimer PS. Mortimer PS. Clin Exp Dermatol. 1995 Mar;20(2):98-106. doi: 10.1111/j.1365-2230.1995.tb02665.x. Clin Exp Dermatol. 1995. PMID: 8565266 Review.
Mapping of primary congenital lymphedema to the 5q35.3 region.
Evans AL, Brice G, Sotirova V, Mortimer P, Beninson J, Burnand K, Rosbotham J, Child A, Sarfarazi M. Evans AL, et al. Among authors: mortimer p. Am J Hum Genet. 1999 Feb;64(2):547-55. doi: 10.1086/302248. Am J Hum Genet. 1999. PMID: 9973292 Free PMC article.
A gene for lymphedema-distichiasis maps to 16q24.3.
Mangion J, Rahman N, Mansour S, Brice G, Rosbotham J, Child AH, Murday VA, Mortimer PS, Barfoot R, Sigurdsson A, Edkins S, Sarfarazi M, Burnand K, Evans AL, Nunan TO, Stratton MR, Jeffery S. Mangion J, et al. Among authors: mortimer ps. Am J Hum Genet. 1999 Aug;65(2):427-32. doi: 10.1086/302500. Am J Hum Genet. 1999. PMID: 10417285 Free PMC article.
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb.
Bell R, Brice G, Child AH, Murday VA, Mansour S, Sandy CJ, Collin JR, Mortimer P, Callen DF, Burnand K. Bell R, et al. Among authors: mortimer p. J Med Genet. 2000 Sep;37(9):725. doi: 10.1136/jmg.37.9.725. J Med Genet. 2000. PMID: 11182939 Free PMC article. No abstract available.
Clinicopathological case 2: lymphoedema-distichiasis syndrome.
Ameen M, Brice G, Mortimer PS. Ameen M, et al. Among authors: mortimer ps. Clin Exp Dermatol. 2003 Jul;28(4):463-4. doi: 10.1046/j.1365-2230.2003.01277.x. Clin Exp Dermatol. 2003. PMID: 12823324 No abstract available.
672 results