Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in theSLC2A10gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01165.x/fullpdf
Reference17 articles.
1. Genetic aspects of human congenital diaphragmatic hernia;Pober;Clin Genet,2008
2. A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin;Zaidi;Eur J Pediatr,2008
3. Three new families with arterial tortuosity syndrome;Wessels;Am J Med Genet A,2004
4. Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families;Callewaert;Hum Mutat,2008
5. A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar;Abdul Wahab;Acta Paediatr,2003
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