K S Roth. Show Affiliations »
Abstract
Mesh: See more » Congenital Abnormalities/etiologyDeafness/etiologyFemaleHumansInfantInfant, NewbornMalePeroxisomal Disorders/complicationsPeroxisomal Disorders/diagnosisPeroxisomal Disorders/physiopathologyPeroxisomal Disorders/therapyPsychomotor Disorders/etiologySeizures/etiology
Year: 1999 PMID: 10047939 DOI: 10.1177/000992289903800202
Source DB: PubMed Journal: Clin Pediatr (Phila) ISSN: 0009-9228 Impact factor: 1.168