Showing results (1-10 of 35) with videos related to
Sort By:
Pageof 4
Annals of the New York Academy of Sciences|June 4, 2008
Phenotypic characterization of primary lymphedemaFiona Connell, Glen Brice, Peter MortimerStroke|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.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.Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
A new locus (GLC1H) for adult-onset primary open-angle glaucoma maps to the 2p15-p16 regionSardha P Suriyapperuma, Anne Child, Trushna Desai, et al.American Journal of Medical Genetics. Part A|April 2, 2010
Lipedema: an inherited conditionAnne H Child, Kristiana D Gordon, Pip Sharpe, et al.American Journal of Medical Genetics. Part A|September 29, 2011
Primary lymphedema with coarctation of the aorta: possible new syndrome or variant of Irons-Bianchi syndrome?John S Ferguson, Shymalar Gunatheesan, Glen Brice, 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.Human Mutation|July 28, 2007
The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutationsPaolo Comeglio, Philip Johnson, Gavin Arno, et al.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|January 17, 2008
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2Tayebeh Rezaie, Rose Ghoroghchian, Rachel Bell, et al.Pageof 4