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Showing articles 0 to 13 of 13 Filter Applied: dysmorphic (Click to remove) Acromegaly NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025 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 Multivessel Cerebral Occlusion in Noonan Syndrome Stroke 56:e359-362, deLima, M.M.,et al, 2025 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Angelman Syndrome Revisited Neurologist 13:305-312, Paprocka,J.,et al, 2007 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 The Epilepsy of Trisomy 9p Neurol 47:821-824, Stern,J.M., 1996 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Fragile X Syndrome:Associated Neurological Abnormalities & Developmental Disabilities Ann Neurol 18:665-669, Wisniewski,K.E.,et al, 1985 Clinicopathological Conference Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983 Fragile X Chromosome & X-Linked Mental Retardation CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982 Clinical Study of Nine Patients with ReNU Syndrome , Okamoto,N.,et al, Showing articles 0 to 13 of 13