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3. Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon. Terwindt GM; Haan J; Ophoff RA; Groenen SM; Storimans CW; Lanser JB; Roos RA; Bleeker-Wagemakers EM; Frants RR; Ferrari MD Brain; 1998 Feb; 121 ( Pt 2)():303-16. PubMed ID: 9549508 [TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant neovascular inflammatory vitreoretinopathy. Bennett SR; Folk JC; Kimura AE; Russell SR; Stone EM; Raphtis EM Ophthalmology; 1990 Sep; 97(9):1125-35; discussion 1135-6. PubMed ID: 2234842 [TBL] [Abstract][Full Text] [Related]
5. The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine. Hottenga JJ; Vanmolkot KR; Kors EE; Kheradmand Kia S; de Jong PT; Haan J; Terwindt GM; Frants RR; Ferrari MD; van den Maagdenberg AM Cephalalgia; 2005 Dec; 25(12):1168-72. PubMed ID: 16305605 [TBL] [Abstract][Full Text] [Related]
6. Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina. van Nouhuys CE Doc Ophthalmol; 1982 Sep; 54(1-4):1-414. PubMed ID: 6897033 [No Abstract] [Full Text] [Related]
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