BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

374 related articles for article (PubMed ID: 11376442)

  • 1. Molecular determinants of atrial and ventricular septal defects and patent ductus arteriosus.
    Vaughan CJ; Basson CT
    Am J Med Genet; 2000; 97(4):304-9. PubMed ID: 11376442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
    Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW
    Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus.
    Howard TD; Guttmacher AE; McKinnon W; Sharma M; McKusick VA; Jabs EW
    Am J Hum Genet; 1997 Dec; 61(6):1405-12. PubMed ID: 9399901
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.
    Satoda M; Zhao F; Diaz GA; Burn J; Goodship J; Davidson HR; Pierpont ME; Gelb BD
    Nat Genet; 2000 May; 25(1):42-6. PubMed ID: 10802654
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic basis of congenital heart disease.
    Gelb BD
    Curr Opin Cardiol; 2004 Mar; 19(2):110-5. PubMed ID: 15075735
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning.
    Zhao F; Bosserhoff AK; Buettner R; Moser M
    PLoS One; 2011; 6(7):e22908. PubMed ID: 21829553
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
    Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
    Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.
    Mani A; Radhakrishnan J; Farhi A; Carew KS; Warnes CA; Nelson-Williams C; Day RW; Pober B; State MW; Lifton RP
    Proc Natl Acad Sci U S A; 2005 Feb; 102(8):2975-9. PubMed ID: 15684060
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Looking down the atrioventricular canal.
    Benson DW; Sund KL
    Cardiovasc Res; 2010 Nov; 88(2):205-6. PubMed ID: 20855523
    [No Abstract]   [Full Text] [Related]  

  • 10. Congenital heart disease caused by mutations in the transcription factor NKX2-5.
    Schott JJ; Benson DW; Basson CT; Pease W; Silberbach GM; Moak JP; Maron BJ; Seidman CE; Seidman JG
    Science; 1998 Jul; 281(5373):108-11. PubMed ID: 9651244
    [TBL] [Abstract][Full Text] [Related]  

  • 11. KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5.
    Darwich R; Li W; Yamak A; Komati H; Andelfinger G; Sun K; Nemer M
    Hum Mol Genet; 2017 Mar; 26(5):942-954. PubMed ID: 28164238
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Holt-Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: functional characterization of a de novo TBX5 mutation.
    Baban A; Pitto L; Pulignani S; Cresci M; Mariani L; Gambacciani C; Digilio MC; Pongiglione G; Albanese S
    Am J Med Genet A; 2014 Jun; 164A(6):1419-24. PubMed ID: 24664498
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare cardiac defect in Holt-Oram syndrome.
    Sinha R; Nema C
    Cardiovasc J Afr; 2012 Mar; 23(2):e3-4. PubMed ID: 22447508
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM; Borlak J
    Hum Mutat; 2004 Jul; 24(1):104. PubMed ID: 15221798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.
    Pabst S; Wollnik B; Rohmann E; Hintz Y; Glänzer K; Vetter H; Nickenig G; Grohé C
    Clin Res Cardiol; 2008 Jan; 97(1):39-42. PubMed ID: 17891520
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial dilated cardiomyopathy associated with pathogenic TBX5 variants: Expanding the cardiac phenotype associated with Holt-Oram syndrome.
    Patterson J; Coats C; McGowan R
    Am J Med Genet A; 2020 Jul; 182(7):1725-1734. PubMed ID: 32449309
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Etiology of congenital heart disease.
    Neill CA
    Cardiovasc Clin; 1972; 4(3):137-47. PubMed ID: 4591014
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel TBX5 duplication in a Japanese family with Holt-Oram syndrome.
    Kimura M; Kikuchi A; Ichinoi N; Kure S
    Pediatr Cardiol; 2015 Jan; 36(1):244-7. PubMed ID: 25274398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic heterogeneity of heart-hand syndromes.
    Basson CT; Solomon SD; Weissman B; MacRae CA; Poznanski AK; Prieto F; Ruiz de la Fuente S; Pease WE; Levin SE; Holmes LB
    Circulation; 1995 Mar; 91(5):1326-9. PubMed ID: 7867169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse.
    Dunlevy L; Bennett M; Slender A; Lana-Elola E; Tybulewicz VL; Fisher EM; Mohun T
    Cardiovasc Res; 2010 Nov; 88(2):287-95. PubMed ID: 20558441
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.