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Annals of the New York Academy of Sciences|June 4, 2008
Phenotypic characterization of primary lymphedemaFiona Connell, Glen Brice, Peter MortimerAmerican 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.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.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.European Journal of Medical Genetics|June 25, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterationsChiara Migliore, Emmanouil Athanasakis, Sophie Dahoun, 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.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2017
Clinical and molecular consequences of disease-associated de novo mutations in SATB2Hemant Bengani, Mark Handley, Mohsan Alvi, et al.Pageof 1