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Results 1 - 5 of 5 for Citrullinemia type II
  1. ... Testing Registry: Citrullinemia type I Genetic Testing Registry: Citrullinemia type II Genetic Testing Registry: Neonatal intrahepatic cholestasis due to ...
  2. ... SOLUTE CARRIER FAMILY 25 (CITRIN), MEMBER 13; SLC25A13 CITRULLINEMIA, TYPE II, NEONATAL-ONSET NCBI Gene ClinVar Kobayashi K, Bang ... Moriyama M, Hsiao KJ, Yang Y. Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: ...
  3. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  4. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
  5. Newborn Screening (National Library of Medicine)  
    Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...