Nucleotide

• Fragile X Syndrome
  Fragile X Syndrome

  A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairm...<br/>Year introduced: 1991(1983)
  MeSH

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on