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Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple café au lait macules, intertriginous freckling, multiple cutaneous neurofibromas, ...
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Neurofibromatosis type 1 (NF1 or also von Recklinghausen's disease), is a tumor predisposition syndrome characterized by the development of typical cutaneous ...
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Neurofibromatosis type 1 (NF1) is a clinically heterogeneous, neurocutaneous genetic disorder characterized by café-au-lait spots, iris Lisch nodules, axillary ...
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NF1. Number of Residues, 2. Details, binding site for residue MG A5 4306. Chain, Residue. A5, A1055. A5, U1056. site_id, NF2. Number of Residues, 2. Details ...
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2007;120(1262):U2731. Shah GN, Bonapace G, Hu PY, et al. Carbonic anhydrase ... Neurofibromatosis. Familial isolated hyperparathyroidism. Hyperparathyroidism ...
Fetisova, N.F. 2008: Medical geography in study of rickettsioses. ... New Zealand Medical Journal 120(1262): U2731 ... Intestinal neurofibromatosis. New Zealand ...
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Sep 1, 2020 · Mutations in RAB39B at Xq28 causes a rare form of X-linked intellectual disability (ID) and Parkinson's disease. Neurofibromatosis type 1 (NF1) ...
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