Author:
Arnold Georgianne L.,Van Hove Johan,Freedenberg Debra,Strauss Arnold,Longo Nicola,Burton Barbara,Garganta Cheryl,Ficicioglu Can,Cederbaum Stephen,Harding Cary,Boles Richard G.,Matern Dietrich,Chakraborty Pranesh,Feigenbaum Annette
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference30 articles.
1. Mutation anaysis in mitochondrial fatty acid oxidation defects, exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype–phenotype relationship;Gregerson;Hum. Mutat.,2001
2. Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors if metabolism;Millington;J. Inherit. Metab. Dis.,1990
3. VLCAD deficiency: Pitfalls in newborn screening and confirmation of diagnosis by mutation analysis;Boneh;Mol. Genet. Metab.,2006
4. Centre for Evidence-Based Medicine, Available from: (accessed May 2, 2008).
5. H.A. Linstone, M. Turof, The Delphi method: techniques and applications, Addison-Wesley Pub. Co., Reading, Mass, 1975, Available from: (accessed online May 1, 2008).
Cited by
134 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献