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Showing articles 0 to 15 of 15 Filter Applied: molecular genetics (Click to remove) Ehlers-Danlos Syndromes BMJ 366:I4966, Ghali, N.,et al, 2019 Zika Virus Associated with Microcephaly NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016 Neurofibromatosis Type 2 Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009 Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009 Tuberous Sclerosis Lancet 372:657-658, Curatolo,P.,et al., 2008 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1 Lancet 361:1552-1554, Reynolds,R.M., et al, 2003 New Developments in the Neurobiology of the Tuberous Sclerosis Complex Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Whipples Disease NEJM 356:55-66, Fenollar,F.,et al, 2007 Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene NEJM 355:831-839, Case 26-2006, 2006 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Showing articles 0 to 15 of 15