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7. Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7q. Kumar A; Olson TM; Thibodeau SN; Michels VV; Schaid DJ; Wallace MR Am J Cardiol; 1994 Dec; 74(12):1281-3. PubMed ID: 7977109 [No Abstract] [Full Text] [Related]
8. [Familial supravalvular aortic stenosis. Investigation in a family and review of the literature]. Burnel P; Marçon F; Lucron H; Bosser G; Gilgenkrantz S; Jonveaux P; Chéry M; Worms AM Arch Mal Coeur Vaiss; 1997 May; 90(5):719-24. PubMed ID: 9295957 [TBL] [Abstract][Full Text] [Related]
9. Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis. Bennett CP; Burn J; Moore GE; Chambers J; Williamson R; Wilkinson J J Med Genet; 1988 May; 25(5):311-2. PubMed ID: 3164411 [TBL] [Abstract][Full Text] [Related]
10. Genetic approaches to cardiovascular disease. Supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome. Keating MT Circulation; 1995 Jul; 92(1):142-7. PubMed ID: 7788908 [TBL] [Abstract][Full Text] [Related]
11. [Genetic diagnosis of Williams syndrome]. Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487 [TBL] [Abstract][Full Text] [Related]
12. Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis. Li DY; Toland AE; Boak BB; Atkinson DL; Ensing GJ; Morris CA; Keating MT Hum Mol Genet; 1997 Jul; 6(7):1021-8. PubMed ID: 9215670 [TBL] [Abstract][Full Text] [Related]
13. Description of a dinucleotide repeat polymorphism in the human elastin gene and its use to confirm assignment of the gene to chromosome 7. Foster K; Ferrell R; King-Underwood L; Povey S; Attwood J; Rennick R; Humphries SE; Henney AM Ann Hum Genet; 1993 May; 57(2):87-96. PubMed ID: 8368807 [TBL] [Abstract][Full Text] [Related]
14. Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis. Tassabehji M; Metcalfe K; Donnai D; Hurst J; Reardon W; Burch M; Read AP Hum Mol Genet; 1997 Jul; 6(7):1029-36. PubMed ID: 9215671 [TBL] [Abstract][Full Text] [Related]
16. Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis. Hayano S; Okuno Y; Tsutsumi M; Inagaki H; Fukasawa Y; Kurahashi H; Kojima S; Takahashi Y; Kato T Int J Cardiol; 2019 Jan; 274():290-295. PubMed ID: 30228022 [TBL] [Abstract][Full Text] [Related]
17. Spectrum of findings in a family with nonsyndromic autosomal dominant supravalvular aortic stenosis: a Doppler echocardiographic study. Ensing GJ; Schmidt MA; Hagler DJ; Michels VV; Carter GA; Feldt RH J Am Coll Cardiol; 1989 Feb; 13(2):413-9. PubMed ID: 2913119 [TBL] [Abstract][Full Text] [Related]
18. Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene. Ewart AK; Jin W; Atkinson D; Morris CA; Keating MT J Clin Invest; 1994 Mar; 93(3):1071-7. PubMed ID: 8132745 [TBL] [Abstract][Full Text] [Related]
19. Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis. Fryssira H; Palmer R; Hallidie-Smith KA; Taylor J; Donnai D; Reardon W J Med Genet; 1997 Apr; 34(4):306-8. PubMed ID: 9138154 [TBL] [Abstract][Full Text] [Related]
20. Congenital heart disease: Molecular diagnostics of supravalvular aortic stenosis. Tassabehji M; Urban Z Methods Mol Med; 2006; 126():129-56. PubMed ID: 16930010 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]