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6. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot. Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173 [TBL] [Abstract][Full Text] [Related]
7. The tetralogy of Fallot-associated G274D mutation impairs folding of the second epidermal growth factor repeat in Jagged-1. Guarnaccia C; Dhir S; Pintar A; Pongor S FEBS J; 2009 Nov; 276(21):6247-57. PubMed ID: 19780835 [TBL] [Abstract][Full Text] [Related]
8. Gene symbol: JAG1. Disease: Alagille syndrome. Conidi ME; Michelucci A; Maggiore G; Simi P Hum Genet; 2008 Oct; 124(3):322. PubMed ID: 18846681 [No Abstract] [Full Text] [Related]
9. Gene symbol: JAG1. Disease: Alagille syndrome. Conidi ME; Michelucci A; Maggiore G; Simi P Hum Genet; 2008 Oct; 124(3):322. PubMed ID: 18846686 [No Abstract] [Full Text] [Related]
10. Gene symbol: JAG1. Disease: Alagille syndrome. Conidi ME; Michelucci A; Maggiore G; Simi P Hum Genet; 2008 Oct; 124(3):321-2. PubMed ID: 18846680 [No Abstract] [Full Text] [Related]
11. Variable expression of Alagille syndrome in a family with a new JAG1 gene mutation. Ziesenitz VC; Loukanov T; Gläser C; Gorenflo M Cardiol Young; 2016 Jan; 26(1):164-7. PubMed ID: 25613755 [TBL] [Abstract][Full Text] [Related]