Volume 14, Issue 2 Our Thanks to Thurza Spring, 2011

First Page		Document Content
Date: 2014-07-15 14:55:37 Biotechnology Rare diseases Motor neurone disease Nervous system Stem cells Hereditary spastic paraplegia Amyotrophic lateral sclerosis Frontotemporal lobar degeneration Primary lateral sclerosis Biology Medicine Health		Volume 14, Issue 2 Our Thanks to Thurza Spring, 2011 Add to Reading List Source URL: sp-foundation.org Download Document from Source Website File Size: 2,72 MB Share Document on Facebook

	Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia DocID: 1uWce - View Document
	Microsoft Word - Monogenic diseases PGD IVIOMICS.doc DocID: 1pc1I - View Document
	* Disclaimer:+The+content+provided+in+this+file+is+for+informational+purposes+only.+Please+consult+your+doctor+ with+any+questions+or+concerns+you+may+have+regarding+a+medical+condition.+ ! !Achondroplasia!!! DocID: 17Sxa - View Document
	The Australian Society for Medical Research NSW Scientific Meeting Instructions for Preparation of Abstracts The selection of contributions for scientific sessions will depend on the quality of the abstract submitted. Au DocID: 15rww - View Document
	The Australian Society for Medical Research NSW Scientific Meeting Instructions for Preparation of Abstracts The selection of contributions for scientific sessions will depend on the quality of the abstract submitted. Au DocID: 12xSY - View Document