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44. Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13. Lyons LA; Martha A; Mintz-Hittner HA; Saunders GF; Ferrell RE Genomics; 1992 Aug; 13(4):925-30. PubMed ID: 1505982 [TBL] [Abstract][Full Text] [Related]
45. Familial atrioventricular septal defect: possible genetic mechanisms. Kumar A; Williams CA; Victorica BE Br Heart J; 1994 Jan; 71(1):79-81. PubMed ID: 8297702 [TBL] [Abstract][Full Text] [Related]
46. A locus for autosomal dominant anterior polar cataract on chromosome 17p. Berry V; Ionides AC; Moore AT; Plant C; Bhattacharya SS; Shiels A Hum Mol Genet; 1996 Mar; 5(3):415-9. PubMed ID: 8852669 [TBL] [Abstract][Full Text] [Related]
47. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1). Brown J; Fingert JH; Taylor CM; Lake M; Sheffield VC; Stone EM Arch Ophthalmol; 1997 Jan; 115(1):95-9. PubMed ID: 9006432 [TBL] [Abstract][Full Text] [Related]
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52. Congenital heart disease in children with Down's syndrome: Turkish experience of 13 years. Nisli K; Oner N; Candan S; Kayserili H; Tansel T; Tireli E; Karaman B; Omeroglu RE; Dindar A; Aydogan U; Başaran S; Ertugrul T Acta Cardiol; 2008 Oct; 63(5):585-9. PubMed ID: 19014001 [TBL] [Abstract][Full Text] [Related]
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60. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21. Boyadjiev SA; Justice CM; Eyaid W; McKusick VA; Lachman RS; Chowdry AB; Jabak M; Zwaan J; Wilson AF; Jabs EW Hum Genet; 2003 Jul; 113(1):1-9. PubMed ID: 12677423 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]