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Phenotypic characterization of primary lymphedema.
Connell F, Brice G, Mortimer P. Connell F, et al. Among authors: brice g. Ann N Y Acad Sci. 2008;1131:140-6. doi: 10.1196/annals.1413.013. Ann N Y Acad Sci. 2008. PMID: 18519967 Review.
Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy.
Rosbotham JL, Brice GW, Child AH, Nunan TO, Mortimer PS, Burnand KG. Rosbotham JL, et al. Among authors: brice gw. Br J Dermatol. 2000 Jan;142(1):148-52. doi: 10.1046/j.1365-2133.2000.03258.x. Br J Dermatol. 2000. PMID: 10651712
A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.
Brice G, Ostergaard P, Jeffery S, Gordon K, Mortimer PS, Mansour S. Brice G, et al. Clin Genet. 2013 Oct;84(4):378-81. doi: 10.1111/cge.12158. Epub 2013 Apr 26. Clin Genet. 2013. PMID: 23550541
A new classification system for primary lymphatic dysplasias based on phenotype.
Connell F, Brice G, Jeffery S, Keeley V, Mortimer P, Mansour S. Connell F, et al. Among authors: brice g. Clin Genet. 2010 May;77(5):438-52. doi: 10.1111/j.1399-0004.2010.01394.x. Clin Genet. 2010. PMID: 20447153
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
Connell FC, Gordon K, Brice G, Keeley V, Jeffery S, Mortimer PS, Mansour S, Ostergaard P. Connell FC, et al. Among authors: brice g. Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub 2013 Jun 27. Clin Genet. 2013. PMID: 23621851 Review.
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene.
Bell R, Brice G, Child AH, Murday VA, Mansour S, Sandy CJ, Collin JR, Brady AF, Callen DF, Burnand K, Mortimer P, Jeffery S. Bell R, et al. Among authors: brice g. Hum Genet. 2001 Jun;108(6):546-51. doi: 10.1007/s004390100528. Hum Genet. 2001. PMID: 11499682
Clinicopathological case 2: lymphoedema-distichiasis syndrome.
Ameen M, Brice G, Mortimer PS. Ameen M, et al. Among authors: brice g. 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.
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. Brice G, et al. J Med Genet. 2002 Jul;39(7):478-83. doi: 10.1136/jmg.39.7.478. J Med Genet. 2002. PMID: 12114478 Free PMC article.
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: brice g. 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: brice g. Am J Hum Genet. 1999 Aug;65(2):427-32. doi: 10.1086/302500. Am J Hum Genet. 1999. PMID: 10417285 Free PMC article.
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