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Journal Abstract Search

135 related items for PubMed ID: 8882398

  • 1. VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothers.
    Froster UG, Wallner SJ, Reusche E, Schwinger E, Rehder H.
    Am J Med Genet; 1996 Mar 15; 62(2):169-72. PubMed ID: 8882398
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  • 2. VACTERL with hydrocephalus: further delineation of the syndrome(s).
    Evans JA, Stranc LC, Kaplan P, Hunter AG.
    Am J Med Genet; 1989 Oct 15; 34(2):177-82. PubMed ID: 2816994
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  • 3. [Vater or Vacterl syndrome (author's transl)].
    Baumann W, Greinacher I, Emmrich P, Spranger J.
    Klin Padiatr; 1976 Jul 15; 188(4):328-37. PubMed ID: 988425
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  • 4. Prenatal diagnosis of sirenomelia with bilateral hydrocephalus: report of a previously undocumented form of VACTERL-H association.
    Onyeije CI, Sherer DM, Handwerker S, Shah L.
    Am J Perinatol; 1998 Mar 15; 15(3):193-7. PubMed ID: 9572377
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  • 7. Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?
    Clementi M, Mammi I, Tenconi R.
    Am J Med Genet; 1997 Jan 10; 68(1):91-3. PubMed ID: 8986284
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  • 9. Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.
    Rossbach HC, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL.
    Am J Med Genet; 1996 Jan 02; 61(1):65-7. PubMed ID: 8741921
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  • 11. [The VACTERL association: a report of a clinical case with hepatic cystic lymphangiectasis].
    Distefano G, Rodonò A, Smilari P, Saporito A, Di Bella D, Magro G, Sanges G, Romeo MG.
    Pediatr Med Chir; 1998 Jan 02; 20(3):223-6. PubMed ID: 9744019
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  • 13. VACTERL-H associated with central hypothyroidism: a case report.
    Aliefendioglu D, Bademci G, Keskil S, Somuncu S, Misirlioglu E, Cakmak AM.
    Genet Couns; 2007 Jan 02; 18(3):331-5. PubMed ID: 18019375
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  • 14. Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus.
    Velazquez D, Pereira E, Havranek T.
    AJP Rep; 2016 Mar 02; 6(1):e74-6. PubMed ID: 26929876
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  • 15. Familial recurrence of tracheoesophageal fistula and associated malformations.
    McMullen KP, Karnes PS, Moir CR, Michels VV.
    Am J Med Genet; 1996 Jun 28; 63(4):525-8. PubMed ID: 8826429
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  • 16. X-linked syndrome of branchial arch and other defects.
    Toriello HV, Higgins JV, Abrahamson J, Waterman DF, Moore WD.
    Am J Med Genet; 1985 May 28; 21(1):137-42. PubMed ID: 4039890
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  • 17. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects.
    Powell CM, Chandra RS, Saal HM.
    Am J Med Genet; 1993 Nov 01; 47(6):807-11. PubMed ID: 8279476
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  • 18. [Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome].
    Salinas-Torres VM, Ramos-Márquez ME, Serra-Ruiz L, Angulo-Castellanos E.
    Arch Argent Pediatr; 2012 Aug 01; 110(4):e67-71. PubMed ID: 22859335
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  • 19. Tethered spinal cord and VACTERL association.
    Kuo MF, Tsai Y, Hsu WM, Chen RS, Tu YK, Wang HS.
    J Neurosurg; 2007 Mar 01; 106(3 Suppl):201-4. PubMed ID: 17465385
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  • 20. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
    Corsello G, Giuffrè L.
    Am J Med Genet; 1994 Jan 01; 49(1):137-8. PubMed ID: 8172244
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