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Showing articles 0 to 11 of 11 Filter Applied: dysmorphic (Click to remove) 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 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification Neurol 87:e56-e57, Saini, A.G.,et al, 2016 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Angelman Syndrome: Clinical Profile J Child Neurol 7:270-280, Zori,R.T.,et al, 1992 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979 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 11 of 11