Peutz-Jeghers syndrome: Difference between revisions

Revision as of 12:51, 26 April 2011 view source Michael (talk \| contribs) 49,316 edits →Clinical: +SCTAT ← Older edit		Revision as of 02:02, 27 September 2011 view source Michael (talk \| contribs) 49,316 edits +abbrev. Newer edit →
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	'''Peutz-Jeghers syndrome''' is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene.		'''Peutz-Jeghers syndrome''', abbreviated '''PJS''', is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene.

	==Clinical==		==Clinical==

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