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Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Brice, G; Mansour, S; Bell, R; Collin, JR; Child, AH; Brady, AF; Sarfarazi, M; Burnand, KG; Jeffery, S; Mortimer, P; et al. Brice, G; Mansour, S; Bell, R; Collin, JR; Child, AH; Brady, AF; Sarfarazi, M; Burnand, KG; Jeffery, S; Mortimer, P; Murday, VA (2002) Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. JOURNAL OF MEDICAL GENETICS, 39 (7). 478 - 483 (6). ISSN 0022-2593 https://doi.org/10.1136/jmg.39.7.478
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: 12114478
Keywords: Abnormalities, Multiple, Adolescent, Adult, Child, Child, Preschool, Chromosomes, Human, Pair 16, DNA-Binding Proteins, Eyelashes, Female, Forkhead Transcription Factors, Genetic Linkage, Humans, Infant, Lymphedema, Lymphography, Male, Phenotype, Puberty, Syndrome, Transcription Factors, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, LYMPHEDEMA-DISTICHIASIS, HEREDITARY LYMPHEDEMA, TRUNCATING MUTATIONS, TRANSCRIPTION FACTOR, HELIX GENE, HETEROGENEITY
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 July 2002Published
Web of Science ID: WOS:000177048100004
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URI: http://openaccess.sgul.ac.uk/id/eprint/2061
Publisher's version: https://doi.org/10.1136/jmg.39.7.478

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