Alagille Syndrome Diagnosis: Revision history

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23 September 2011

22 September 2011

  • curprev 03:1303:13, 22 September 2011Sandeepbasnet2 talk contribs 3,303 bytes +3,303 Created page with "The diagnosis is primarily clinical .Sequence analysis of ''JAG1'' detects mutation in 90% of individuals with symptoms. Around 7% of affected individuals have microdeletion of 2..."