Recurrent fetal polycystic kidneys associated with glutaric aciduria type II
Author:
Publisher
Wiley
Subject
Microbiology (medical),General Medicine,Immunology and Allergy,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1699-0463.1998.tb00276.x/fullpdf
Reference16 articles.
1. Lethal multiple acyl-CoA dehydrogenase deficiency with dysmorphic features;Bennett;J. Inherited Metab. Dis.,1987
2. Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria;Boué;Lancet,1984
3. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers;Böhm;Eur. J. Pediatr.,1982
4. The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MS;Chalmers;J. Inherited Metab. Dis.,1985
5. Glutaric aciduria type II: Evidence for a defect related to the electron transfer flavoprotein or its dehydrogenase;Christensen;Pediatr. Res.,1984
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