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    NCBI Reference Sequence: XP_015628973.1 (click to see this obsolete version)

    • Record suppressed. This record was removed as a result of standard genome annotation processing. Please see www.ncbi.nlm.nih.gov/genome/annotation_euk/process/ for more information.

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    • Congenital Hypothyroidism
      Congenital Hypothyroidism
      A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis ...<br/>Year introduced: 2006 (1966)
      MeSH

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