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23. [Phakomatosis pigmentovascularis (type IIIa)]. Stadhouders-Keet SA; Glastra A; Van Vloten WA Ned Tijdschr Geneeskd; 1999 Jun; 143(25):1337. PubMed ID: 10454887 [No Abstract] [Full Text] [Related]
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25. [Cowden's disease (multiple hamartoma syndrome). Review of the literature in connection with 1 case]. Civatte J; Laufer J; Delort J; Belaich S; Morel P Ann Med Interne (Paris); 1978 Oct; 129(10):593-9. PubMed ID: 369427 [No Abstract] [Full Text] [Related]
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28. [A case of Schimmelpenning-Feuerstein-Mims' syndrome sith gradual development of cataract]. Leyh F; Loewel R Z Hautkr; 1973 Sep; 48(17):695-8. PubMed ID: 4205126 [No Abstract] [Full Text] [Related]
33. [Hereditary myatrophical ataxia--syndrome or diagnosis? Critical remarks on the nosology of hereditary degenerative diseases from the viewpoint of medical genetics]. Lietz S; Wittwer B Psychiatr Neurol Med Psychol (Leipz); 1973 Feb; 25(2):65-73. PubMed ID: 4197354 [No Abstract] [Full Text] [Related]
39. Unilateral Lisch nodules in a 47-year-old woman without other stigmata of neurofibromatosis type I: an example of segmental neurofibromatosis? Nicita F; Iannetti L; Spalice A; Papetti L; Ursitti F; Properzi E; Ruggieri M Ophthalmic Genet; 2013 Sep; 34(3):178-9. PubMed ID: 23205842 [No Abstract] [Full Text] [Related]
40. [Tuberous sclerosis of Bourneville: contribution of the ophthalmologist in 2 cases]. Caujolle JP; Grandon M; Gramet C; Guez JE; Lods F Bull Soc Ophtalmol Fr; 1989 Mar; 89(3):473-7. PubMed ID: 2513136 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]