Enter your terms above and click the 'Search' button.

Showing articles 0 to 8 of 8 Filter Applied: molecular genetics (Click to remove) Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009 Spinal Muscular Atrophy Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008 What Level of Care for the Neurofibromatoses? Lancet 353:1114-1116, Huson,S.M., 1999 The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2 JAMA 278:51-57, Gutmann,D.H.,et al, 1997 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm JNNP 86:774-781, Van Egmond, M.E.,et al, 2015 Practice Parameter: Evaluation of the Child with Global Developmental Delay Neurol 60:367-380, Shevell,M.,et al, 2003 Molecular Genetics of Duchenne and Becker Muscular Dystrophy J Pediatr 117:1-15, Darras,B.T., 1990 Showing articles 0 to 8 of 8