BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

34 related articles for article (PubMed ID: 17615644)

  • 1. Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
    Selamet Tierney ES; Marans Z; Rutkin MB; Chung WK
    Cardiol Young; 2007 Jun; 17(3):268-74. PubMed ID: 17445335
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional study of DAND5 variant in patients with Congenital Heart Disease and laterality defects.
    Cristo F; Inácio JM; de Almeida S; Mendes P; Martins DS; Maio J; Anjos R; Belo JA
    BMC Med Genet; 2017 Jul; 18(1):77. PubMed ID: 28738792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.
    Ozcelik C; Bit-Avragim N; Panek A; Gaio U; Geier C; Lange PE; Dietz R; Posch MG; Perrot A; Stiller B
    Pediatr Cardiol; 2006; 27(6):695-8. PubMed ID: 17072672
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Generation of human iPSC line from a patient with laterality defects and associated congenital heart anomalies carrying a DAND5 missense alteration.
    Cristo F; Inácio JM; Rosas G; Carreira IM; Melo JB; de Almeida LP; Mendes P; Martins DS; Maio J; Anjos R; Belo JA
    Stem Cell Res; 2017 Dec; 25():152-156. PubMed ID: 29136563
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel and recurrent JAG1 mutations in patients with tetralogy of Fallot.
    Guida V; Chiappe F; Ferese R; Usala G; Maestrale G; Iannascoli C; Bellacchio E; Mingarelli R; Digilio MC; Marino B; Uda M; De Luca A; Dallapiccola B
    Clin Genet; 2011 Dec; 80(6):591-4. PubMed ID: 22040217
    [No Abstract]   [Full Text] [Related]  

  • 6. Searching for order among disorders of laterality.
    McElhinney DB
    Cardiol Young; 2007 Jun; 17(3):264-7. PubMed ID: 17615644
    [No Abstract]   [Full Text] [Related]  

  • 7. Genes in congenital heart disease: atrioventricular valve formation.
    Joziasse IC; van de Smagt JJ; Smith K; Bakkers J; Sieswerda GJ; Mulder BJ; Doevendans PA
    Basic Res Cardiol; 2008 May; 103(3):216-27. PubMed ID: 18392768
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homeodomain factor Nkx2-5 in heart development and disease.
    Harvey RP; Lai D; Elliott D; Biben C; Solloway M; Prall O; Stennard F; Schindeler A; Groves N; Lavulo L; Hyun C; Yeoh T; Costa M; Furtado M; Kirk E
    Cold Spring Harb Symp Quant Biol; 2002; 67():107-14. PubMed ID: 12858530
    [No Abstract]   [Full Text] [Related]  

  • 9. [Systems controlling limb tissue patterning].
    Shiraishi Y; Kuroiwa A
    Tanpakushitsu Kakusan Koso; 2005 May; 50(6 Suppl):638-43. PubMed ID: 15926493
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetic and Developmental Basis of Cardiovascular Malformations.
    Azhar M; Ware SM
    Clin Perinatol; 2016 Mar; 43(1):39-53. PubMed ID: 26876120
    [TBL] [Abstract][Full Text] [Related]  

  • 11. From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases.
    Cecchetto A; Rampazzo A; Angelini A; Bianco LD; Padalino M; Stellin G; Daliento L
    Future Cardiol; 2010 May; 6(3):373-93. PubMed ID: 20462343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Knowing left from right: the molecular basis of laterality defects.
    Capdevila I; Izpisúa Belmonte JC
    Mol Med Today; 2000 Mar; 6(3):112-8. PubMed ID: 10689314
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 15.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.