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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 4 |
2024 | 0 |
Search Results
4 results
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Page 1
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub 2013 Jun 27.
Clin Genet. 2013.
PMID: 23621851
Review.
FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.
Gordon K, Spiden SL, Connell FC, Brice G, Cottrell S, Short J, Taylor R, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.
Gordon K, et al.
Hum Mutat. 2013 Jan;34(1):23-31. doi: 10.1002/humu.22223. Epub 2012 Oct 16.
Hum Mutat. 2013.
PMID: 23074044
Review.
Item in Clipboard
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
Item in Clipboard
Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.
Gordon K, Schulte D, Brice G, Simpson MA, Roukens MG, van Impel A, Connell F, Kalidas K, Jeffery S, Mortimer PS, Mansour S, Schulte-Merker S, Ostergaard P.
Gordon K, et al.
Circ Res. 2013 Mar 15;112(6):956-60. doi: 10.1161/CIRCRESAHA.113.300350. Epub 2013 Feb 14.
Circ Res. 2013.
PMID: 23410910
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