72 MUONNET H J[removed]

First Page		Document Content
Date: 2014-04-25 15:36:35 Rare diseases Fibrodysplasia ossificans progressiva Harry Raymond Eastlack ACVR1 Ossification Bone morphogenetic protein 4 Bone disease Osteoporosis Health Biology International FOP Association		72 MUONNET H J[removed] Add to Reading List Source URL: newsroom.aaos.org Download Document from Source Website File Size: 684,68 KB Share Document on Facebook

	Microsoft Word - Masters project 1.docx DocID: 1oDL1 - View Document
	B R I E F C O M M U N I C AT I O N S A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia DocID: 16SsQ - View Document
	A novel regulatory mechanism of the BMP signaling pathway Jose Maria Amich Manero Oak House School, Barcelona, Spain under the direction of Prof. Vicki Rosen Dr. Jonathan Lowery DocID: xz2I - View Document
	A novel regulatory mechanism of the BMP signaling pathway Jose Maria Amich Manero Oak House School, Barcelona, Spain under the direction of Prof. Vicki Rosen Dr. Jonathan Lowery DocID: xpPi - View Document
	72 MUONNET H J[removed] DocID: svTq - View Document