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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
92 related items for PubMed ID: 3238297
1. [Stickler syndrome. Apropos of a case]. Ziegler G, Gastaud P, Euller-Ziegler L, De Galleani B. Rev Rhum Mal Osteoartic; 1988 Dec; 55(12):1009-10. PubMed ID: 3238297 [No Abstract] [Full Text] [Related]
2. [Goldman-Favre hyaloid-tapeto-retinal degeneration]. Neetens A, Burvenich H, Hendrata Y, Van Rompaey J, Hofkens R. Bull Mem Soc Fr Ophtalmol; 1980 Dec; 92():185-90. PubMed ID: 6971684 [No Abstract] [Full Text] [Related]
6. Kniest (Wagner-Stickler variant) and Goldmann-Favre disease in one sibship. Neetens A. Bull Soc Belge Ophtalmol; 1987 Dec; 223 Pt 2():27-32. PubMed ID: 3502790 [No Abstract] [Full Text] [Related]
7. Leri-Weill syndrome (dyschondrosteosis): a family study. Mohan V, Gupta RP, Helmi K, Marklund T. J Hand Surg Br; 1988 Feb; 13(1):16-8. PubMed ID: 3361200 [Abstract] [Full Text] [Related]
8. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy]. Vallat M, Fritsch D, Van Coppenolle F, Detre J, Moze M, Rabourdin F. J Fr Ophtalmol; 1985 Feb; 8(4):301-7. PubMed ID: 4020040 [Abstract] [Full Text] [Related]
9. A family with vitreo-tapeto-retino-choroidal degeneration with dominant transmission. Wille H. Acta Ophthalmol (Copenh); 1980 Feb; 58(1):148-57. PubMed ID: 6967673 [Abstract] [Full Text] [Related]
10. Vitreous veils and radial lattice in Marshall syndrome. Brubaker JW, Mohney BG, Pulido JS, Babovic-Vuksanovic D. Ophthalmic Genet; 2008 Dec; 29(4):184-5. PubMed ID: 19005991 [Abstract] [Full Text] [Related]
11. Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance. MacDermot KD, Roth SC, Hall C, Winter RM. J Med Genet; 1987 Oct; 24(10):602-8. PubMed ID: 3681905 [Abstract] [Full Text] [Related]