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6. Electron microscopy as an aid to diagnosis of disorders of the extracellular matrix: a new type of spondyloepiphyseal dysplasia. Byers PH; Holbrook KA; Chandler JW; Bornstein P; Hall JG Birth Defects Orig Artic Ser; 1978; 14(6B):221-32. PubMed ID: 310322 [No Abstract] [Full Text] [Related]
8. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome. Meretoja J Ann Clin Res; 1969 Dec; 1(4):314-24. PubMed ID: 4313418 [No Abstract] [Full Text] [Related]
9. [Follicular atrophoderma, hypotrichosis, and multiple milia associated with minimal osteo-cartilaginous dystrophies. Familial study of 3 cases]. Meynadier J; Guilhou JJ; Barnéon G; Malbos S; Guillot B Ann Dermatol Venereol; 1979 May; 106(5):497-501. PubMed ID: 496212 [No Abstract] [Full Text] [Related]
10. [Contribution to the knowledge of spotted dystrophy of the corneal parenchyma. (Speckled dystrophy of François and Neetens)]. Toselli C; Volpi U; Pirodda A Ann Ottalmol Clin Ocul; 1966 Sep; 92(9):770-4. PubMed ID: 5300513 [No Abstract] [Full Text] [Related]
13. [Identification of BIGH3 gene mutations in the patients with two types of corneal dystrophies]. Jin T; Zou LH; Yang L; Dong WL; Yu J; Lu L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):32-4. PubMed ID: 14767905 [TBL] [Abstract][Full Text] [Related]
14. [Hereditary and familial nodular degeneration of the cornea. Groenouw's disease. 3 cases in 3 generations]. Pestre A Bull Soc Ophtalmol Fr; 1971 Dec; 71(12):1029-33. PubMed ID: 4949335 [No Abstract] [Full Text] [Related]