Author:
Kumari Chandrawati,Singh Ankur,Ramji Siddharth,Shoemaker James D.,Kapoor Seema
Publisher
Springer Science and Business Media LLC
Reference17 articles.
1. Saudubray JM. Clinical phenotype: diagnosis/algorithms. In: Scriver CBA, Sly W, Valle D, editors. The metabolic and molecular bases of inherited disease. New York: McGraw Hill; 2001. p. 1327–402.
2. Tanaka K, Budd MA, Efron ML, Isselbacher KJ. Isovaleric acidemia: a new genetic defect of leucine metabolism. Proc Natl Acad Sci USA. 1966;56(1):236–42.
3. Bjorkman L, McLean C, Steen G. Organic acids in urine from human newborns. Clin Chem. 1976;22(1):49–52.
4. Mills GA, Walker V. Urinary excretion of cyclohexanediol, a metabolite of the solvent cyclohexanone, by infants in a special care unit. Clin Chem. 1990;36(6):870–4.
5. Guneral F, Bachmann C. Age-related reference values for urinary organic acids in a healthy Turkish pediatric population. Clin Chem. 1994;40(6):862–6.
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