Lymphedema-distichiasis syndrome and FOXC2 gene mutation
- 1 October 2002
- journal article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 134 (4) , 592-596
- https://doi.org/10.1016/s0002-9394(02)01642-2
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsJournal of Medical Genetics, 2001
- Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the geneHuman Genetics, 2001
- A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the EyeAmerican Journal of Human Genetics, 2001
- Mapping of the Locus for Cholestasis-Lymphedema Syndrome (Aagenaes Syndrome) to a 6.6-cM Interval on Chromosome 15qAmerican Journal of Human Genetics, 2000
- Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine KinaseAmerican Journal of Human Genetics, 2000
- Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25European Journal of Human Genetics, 2000
- A Gene for Lymphedema-Distichiasis Maps to 16q24.3American Journal of Human Genetics, 1999
- Distichiasis and Cleft PalatePlastic and Reconstructive Surgery, 1989
- Distichiasis, congenital heart defects and mixed peripheral vascular anomaliesAmerican Journal of Medical Genetics, 1985
- Hereditary spinal arachnoid cysts, distichiasis, and lymphedemaAnnals of Neurology, 1980