Loading...
Reach Banner
Keywords
Last name
Institution

Connection

Search Results to

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following properties of Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014).

PropertyValue
has minor subject area list Alleles; Amidohydrolases; Biotin; Biotinidase; Child; Child, Preschool; Disease Management; Female; Genetic Association Studies; Hearing Loss; Heterozygote; Homozygote; Humans; Infant; Infant, Newborn; Male; Mutation; Ontario; Pilot Projects

Search criteria
  • Project
  • Management