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Showing articles 0 to 10 of 10 Filter Applied: dysmorphic (Click to remove) Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum Ann Neurol 97:611-628, Coppens,S.,et al, 2025 A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium Neurol 100:631-637, Zeng,T.f.,et al, 2023 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Fragile X Chromosome & X-Linked Mental Retardation CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982 Showing articles 0 to 10 of 10