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Journal Abstract Search

361 related items for PubMed ID: 8172244

  • 1. 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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  • 3. X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
    Genuardi M, Chiurazzi P, Capelli A, Neri G.
    Birth Defects Orig Artic Ser; 1993 Jan 01; 29(1):235-41. PubMed ID: 8280876
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  • 4. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
    Hsia YE, Bratu M, Herbordt A.
    Pediatrics; 1971 Aug 01; 48(2):237-47. PubMed ID: 4997860
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  • 9. VACTERL-H associated with central hypothyroidism: a case report.
    Aliefendioglu D, Bademci G, Keskil S, Somuncu S, Misirlioglu E, Cakmak AM.
    Genet Couns; 2007 Aug 01; 18(3):331-5. PubMed ID: 18019375
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  • 10. VATER association (a case report).
    Bhandari B, Ajmera NK, Tak SK, Khurana R.
    Indian Pediatr; 1979 Dec 01; 16(12):1133-5. PubMed ID: 541080
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  • 12. [Concomitant anomalies in developmental defects of the rectum and anus in children].
    Arnaudov D, Apostolov A.
    Khirurgiia (Mosk); 1972 Jun 01; 48(6):99-100. PubMed ID: 4261346
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  • 13. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
    Wang H, Hunter AG, Clifford B, McLaughlin M, Thompson D.
    Am J Med Genet; 1993 Aug 01; 47(1):114-7. PubMed ID: 8368240
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  • 14. Triphalangeal thumb in a case of VACTERL-hydrocephalus association.
    Balci S, Senocak ME, Derbent M.
    Genet Couns; 2003 Aug 01; 14(2):257-8. PubMed ID: 12872824
    [No Abstract] [Full Text] [Related]

  • 15. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O, Ozer EA, Ozer A, Aydinlioglu H, Helvaci M.
    Genet Couns; 2007 Aug 01; 18(2):247-50. PubMed ID: 17710878
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  • 18. Genetic syndrome suspicion: examples of clinical approach in the neonatal unit.
    Giuffrè M, De Sanctis L.
    Minerva Pediatr; 2010 Jun 01; 62(3 Suppl 1):199-201. PubMed ID: 21089741
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  • 19. Diagnostic criteria for Walker-Warburg syndrome.
    Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M.
    Am J Med Genet; 1989 Feb 01; 32(2):195-210. PubMed ID: 2494887
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