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Edited by Aldo Campana,
February 8, 2010
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17q11.2, 2p22-p21 GeneReviews Google OMIM Orphanet PubMed Wikipedia [Cardiovascular system] [Digestive system] [Eyes] [FSNF] [NF1 microdeletion syndrome] [NF2] [NFNS] [Nervous system] [Pheochromocytoma] [Segmental neurofibromatosis] [Skeletal system] [Skin - Histology] [Urogenital system] Neurofibromatosis, type I *Gene map locus 17q11.2, 2p22-p21 NF1 Neurofibromatosis Von Recklinghausen disease [Clinical features: multiple neurofibromas; café-au-lait spots; iris Lisch nodules] [Inheritance: autosomal dominant] |
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58 images [ from 61 to 58 ] |
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