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Showing articles 0 to 13 of 13 Filter Applied: dysmorphic (Click to remove) Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Multivessel Cerebral Occlusion in Noonan Syndrome Stroke 56:e359-362, deLima, M.M.,et al, 2025 Acromegaly NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema Adams & Victors Principles of Neurology Chp 40, pg 1156, Ropper, A.H.,et al, 2014 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,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 Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship Neurol 33:267-277, Stein,S.A.,et al, 1983 Fragile X Chromosome & X-Linked Mental Retardation CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Showing articles 0 to 13 of 13