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Annals of the New York Academy of Sciences|June 4, 2008
Phenotypic characterization of primary lymphedemaFiona Connell, Glen Brice, Peter Mortimer
Human Genetics|November 14, 2009
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasiaFiona Connell, Kamini Kalidas, Pia Ostergaard, et al.
European Journal of Human Genetics : EJHG|March 26, 2015
The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature reviewGiles Atton, Kristiana Gordon, Glen Brice, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Congenital vascular malformations: a series of five prenatally diagnosed casesFiona Connell, Tessa Homfray, Baskaran Thilaganathan, et al.
European Journal of Human Genetics : EJHG|August 6, 2015
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndromeSarah Joyce, Kristiana Gordon, Glen Brice, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
European Journal of Human Genetics : EJHG|January 17, 2008
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2Tayebeh Rezaie, Rose Ghoroghchian, Rachel Bell, et al.
Human Genetics|May 21, 2005
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutationsCarolyn Sholto-Douglas-Vernon, Rachel Bell, Glen Brice, et al.
Circulation Research|February 16, 2013
Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedemaKristiana Gordon, Dörte Schulte, Glen Brice, et al.
Stroke|February 20, 2010
Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individualsPoneh Adib-Samii, Glen Brice, Roswell J Martin, et al.
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