Lymphedema, cardiac septal defects, and characteristic facies: Possible new case of Irons–Bianchi syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.31949/fullpdf
Reference8 articles.
1. Milroy disease and the VEGFR-3 mutation phenotype
2. Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
3. Truncating mutations in FOXC2 cause multiple lymphedema syndromes
4. Noonan syndrome and its related disorders
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1. Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons-Bianchi syndrome?;American Journal of Medical Genetics Part A;2011-09-22
2. 4 Lymfoedeem;Oedeem en oedeemtherapie;2011
3. Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome?;American Journal of Medical Genetics Part A;2010-06-25
4. Massive lymphedema, atrial septal defect, mild mental retardation: Possible case of Irons-Bianchi syndrome;American Journal of Medical Genetics Part A;2009-06-16
5. Literature Watch;Lymphatic Research and Biology;2007-12
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