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Milroy disease and the VEGFR-3 mutation phenotype

Brice, G; Child, AH; Evans, A; Bell, R; Mansour, S; Burnand, K; Sarfarazi, M; Jeffery, S; Mortimer, P (2005) Milroy disease and the VEGFR-3 mutation phenotype. JOURNAL OF MEDICAL GENETICS, 42 (2). 98 - 102 (5). ISSN 0022-2593 https://doi.org/10.1136/jmg.2004.024802
SGUL Authors: Child, Anne Hawthorne Jeffery, Stephen Mortimer, Peter Sydney Mansour, Sahar Brice, Glen Worthington

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Item Type: Article
Additional Information: PubMed ID: 15689446
Keywords: Adult, Age of Onset, Female, Heterozygote Detection, Humans, Lymphedema, Male, Mutation, Nails, Malformed, Papilloma, Phenotype, Saphenous Vein, Urogenital Abnormalities, Varicose Veins, Vascular Endothelial Growth Factor Receptor-3, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, LYMPHEDEMA-DISTICHIASIS SYNDROME, PRIMARY CONGENITAL LYMPHEDEMA, HEREDITARY LYMPHEDEMA, GENETIC-HETEROGENEITY, TRANSCRIPTION FACTOR, FOXC2 MUTATIONS, FAMILIES, LINKAGE, LYMPHANGIOGENESIS, RECEPTOR-3
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cardiac (INCCCA)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: JOURNAL OF MEDICAL GENETICS
ISSN: 0022-2593
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Dates:
DateEvent
1 February 2005Published
Web of Science ID: WOS:000226748100002
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URI: https://openaccess.sgul.ac.uk/id/eprint/2580
Publisher's version: https://doi.org/10.1136/jmg.2004.024802

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