BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 19822228)

  • 41. Notochord anomalies in the adriamycin rat model: A morphologic and molecular basis for the VACTERL association.
    Gillick J; Mooney E; Giles S; Bannigan J; Puri P
    J Pediatr Surg; 2003 Mar; 38(3):469-73; discussion 469-73. PubMed ID: 12632369
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A role for sonic hedgehog signaling in the pathogenesis of human tracheoesophageal fistula.
    Spilde T; Bhatia A; Ostlie D; Marosky J; Holcomb G; Snyder C; Gittes G
    J Pediatr Surg; 2003 Mar; 38(3):465-8. PubMed ID: 12632368
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Likelihood of meeting defined VATER/VACTERL phenotype in infants with esophageal atresia with or without tracheoesophageal fistula.
    Guptha S; Shumate C; Scheuerle AE
    Am J Med Genet A; 2019 Nov; 179(11):2202-2206. PubMed ID: 31436871
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Malrotation in conjunction with esophageal atresia/tracheo-esophageal fistula.
    Cieri MV; Arnold GL; Torfs CP
    Teratology; 1999 Sep; 60(3):114-6. PubMed ID: 10471893
    [TBL] [Abstract][Full Text] [Related]  

  • 45. An Incidental Finding of Butterfly Vertebrae in a Case of Vertebral Defects, Anal Atresia, Cardiac Defects, Tracheo-Esophageal Fistula, Renal Anomalies, and Limb Abnormalities (VACTERL).
    Rao A; Gaikwad S; Taksande A; Wanjari MB
    Cureus; 2023 Jan; 15(1):e33401. PubMed ID: 36751248
    [TBL] [Abstract][Full Text] [Related]  

  • 46. VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis.
    Corsello G; Maresi E; Corrao AM; Dimita U; Lo Cascio M; Cammarata M; Giuffrè L
    Am J Med Genet; 1992 Dec; 44(6):813-5. PubMed ID: 1481853
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Etiology of esophageal atresia and tracheoesophageal fistula: "mind the gap".
    de Jong EM; Felix JF; de Klein A; Tibboel D
    Curr Gastroenterol Rep; 2010 Jun; 12(3):215-22. PubMed ID: 20425471
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Oesophageal atresia.
    Spitz L
    Orphanet J Rare Dis; 2007 May; 2():24. PubMed ID: 17498283
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Tracheal agenesis and associated malformations: a comparison with tracheoesophageal fistula and the VACTERL association.
    Evans JA; Reggin J; Greenberg C
    Am J Med Genet; 1985 May; 21(1):21-38. PubMed ID: 4003446
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Patients with anorectal malformation and upper limb anomalies: genetic evaluation is warranted.
    van den Hondel D; Wijers CH; van Bever Y; de Klein A; Marcelis CL; de Blaauw I; Sloots CE; IJsselstijn H
    Eur J Pediatr; 2016 Apr; 175(4):489-97. PubMed ID: 26498647
    [TBL] [Abstract][Full Text] [Related]  

  • 51. De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations.
    Dworschak GC; Draaken M; Marcelis C; de Blaauw I; Pfundt R; van Rooij IA; Bartels E; Hilger A; Jenetzky E; Schmiedeke E; Grasshoff-Derr S; Schmidt D; Märzheuser S; Hosie S; Weih S; Holland-Cunz S; Palta M; Leonhardt J; Schäfer M; Kujath C; Rissmann A; Nöthen MM; Zwink N; Ludwig M; Reutter H
    Am J Med Genet A; 2013 Dec; 161A(12):3035-41. PubMed ID: 24038947
    [TBL] [Abstract][Full Text] [Related]  

  • 52. ESOPHAGEAL ATRESIA WITH RECURRENT TRACHEOESOPHAGEAL FISTULAS AND MICRODUPLICATION 22q11.23.
    Puvabanditsin S; Garrow E; February M; Yen E; Mehta R
    Genet Couns; 2015; 26(3):313-20. PubMed ID: 26625662
    [TBL] [Abstract][Full Text] [Related]  

  • 53. VACTERL-H associated with central hypothyroidism: a case report.
    Aliefendioglu D; Bademci G; Keskil S; Somuncu S; Misirlioglu E; Cakmak AM
    Genet Couns; 2007; 18(3):331-5. PubMed ID: 18019375
    [TBL] [Abstract][Full Text] [Related]  

  • 54. McKusick-Kaufman syndrome associated with esophageal atresia and distal tracheoesophageal fistula: a case report and review of the literature.
    Pul N; Pul M; Gedik Y
    Am J Med Genet; 1994 Feb; 49(3):341-3. PubMed ID: 8209897
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genetics and developmental biology of oesophageal atresia and tracheo-oesophageal fistula: lessons from mice relevant for paediatric surgeons.
    Felix JF; Keijzer R; van Dooren MF; Rottier RJ; Tibboel D
    Pediatr Surg Int; 2004 Oct; 20(10):731-6. PubMed ID: 15517294
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
    Layman-Pleet L; Jackson CC; Chou S; Boycott KM
    J Pediatr Surg; 2007 Sep; 42(9):E1-3. PubMed ID: 17848225
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Associated malformations in patients with esophageal atresia.
    Stoll C; Alembik Y; Dott B; Roth MP
    Eur J Med Genet; 2009; 52(5):287-90. PubMed ID: 19410022
    [TBL] [Abstract][Full Text] [Related]  

  • 58. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
    Corsello G; Giuffrè L
    Am J Med Genet; 1994 Jan; 49(1):137-8. PubMed ID: 8172244
    [No Abstract]   [Full Text] [Related]  

  • 59. Feingold syndrome: clinical review and genetic mapping.
    Celli J; van Bokhoven H; Brunner HG
    Am J Med Genet A; 2003 Nov; 122A(4):294-300. PubMed ID: 14518066
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Brain abnormality within the scope of a VACTERL association].
    Nikischin W; Krolikowski I; Santer R
    Monatsschr Kinderheilkd; 1991 Jun; 139(6):360-2. PubMed ID: 1896049
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.