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
Related URLs:	Author
Dates:	Date Event 1 July 2002 Published
Web of Science ID:	WOS:000177048100004
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URI:	https://openaccess.sgul.ac.uk/id/eprint/2061
Publisher's version:	https://doi.org/10.1136/jmg.39.7.478

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