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
Full text not available from this repository.
| Item Type: |
Article
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| 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 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 February 2005 | Published |
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| 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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