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17q11.2 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 NF1 Neurofibromatosis Von Recklinghausen disease [Clinical features: multiple neurofibromas; café-au-lait spots; iris Lisch nodules] [Inheritance: autosomal dominant] |
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Plexiform Neurofibromatosis |
Skin: Neurofibromatosis |
Skin: Neurofibromatosis |
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Indian Pediatrics |
IPLAB.net |
IPLAB.net |
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NF1: neurofibromas |
Plexiform neurofibroma |
Neurofibroma |
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Medical Genetics |
Medical Genetics |
MedlinePlus |
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Edited by Aldo Campana,
August 21, 2012
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