Tan, April W <br/><br/>
Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.  [electronic resource] 

 -  Fetal and pediatric pathology  Aug 2018 
 - 296-300 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1551-3823 
<br/><br/><label>Standard No.: </label>10.1080/15513815.2018.1485797  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ankyrins--deficiency<br/>Codon, Nonsense<br/>Female<br/>Hispanic or Latino--genetics<br/>Humans<br/>Hyperbilirubinemia, Neonatal--genetics<br/>Infant, Newborn<br/>Spherocytosis, Hereditary--complications