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![]() Date: 2013-09-16 18:32:42Genetic genealogy Medical genetics HMG-CoA Rare diseases Protein families Newborn screening Fatty-acid metabolism disorder Health 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase | Add to Reading List |
![]() | POSTER SESSIONS The LIPID MAPS meeting features two poster sessions with 44 posters. Of these, twelve were selected for lightning talks (see program) by the review committee, consisting of Susan A. Henry, Alfred H. MerriDocID: 19Ufx - View Document |
![]() | What is Carnitine ? Nelson LS Tang, MBChB, FRCPA Associate Professor Department of Chemical Pathology The Chinese University of Hong KongDocID: 13Fs6 - View Document |
![]() | Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findingsDocID: 12jOC - View Document |
![]() | Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition IncidenceDocID: Z5KR - View Document |
![]() | Disorders and Reference RangesDocID: KTuv - View Document |