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Journal Abstract Search

106 related items for PubMed ID: 6214946

  • 1. A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.
    Fellous M, Boué J, Malbrunot C, Wollman E, Sasportes M, Van Cong N, Marcelli A, Rebourcet R, Hubert C, Demenais F, Elston RC, Namboodiri KK, Kaplan EB, Fellous M.
    Am J Med Genet; 1982 Aug; 12(4):465-87. PubMed ID: 6214946
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  • 2. [Segregation of HLA haplotypes in a family with infants having spina bifida].
    Kulakowski S, Delire M, De Bruyere M.
    J Genet Hum; 1979 Oct; 27(3):205-19. PubMed ID: 395274
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  • 5. Spina bifida occulta: is it a predictor of underlying spinal cord abnormality in patients with lower urinary tract dysfunction?
    Nejat F, Radmanesh F, Ansari S, Tajik P, Kajbafzadeh A, El Khashab M.
    J Neurosurg Pediatr; 2008 Feb; 1(2):114-7. PubMed ID: 18352778
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  • 11. Radiographic method to assess the prevalence of sacral spina bifida occulta.
    Albrecht TL, Scutter SD, Henneberg M.
    Clin Anat; 2007 Mar; 20(2):170-4. PubMed ID: 16941459
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  • 13. Sacral fatigue fractures in children with sacral spina bifida occulta.
    Hama S, Takata Y, Sakai T, Higashino K, Abe M, Nagamachi A, Sairyo K.
    J Pediatr Orthop B; 2016 May; 25(3):278-82. PubMed ID: 26196371
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  • 15. [Spina bifida occulta and other neural tube defects. Genetic study and management].
    Robert E.
    Neurochirurgie; 1988 May; 34 Suppl 1():87-90. PubMed ID: 3054614
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  • 16. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
    Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T.
    Nat Genet; 1998 Dec; 20(4):358-61. PubMed ID: 9843207
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  • 17. Lumbosacral transitional vertebra associated with sacral spina bifida occulta: a case report.
    George P, Maria T, Panagiotis K.
    Acta Medica (Hradec Kralove); 2013 Dec; 56(3):126-9. PubMed ID: 24592751
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  • 18. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
    Ramprasad VL, Thool A, Murugan S, Nancarrow D, Vyas P, Rao SK, Vidhya A, Ravishankar K, Kumaramanickavel G.
    Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):17-23. PubMed ID: 15623749
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  • 19. [Epidemiologic and genetic studies of spina bifida (author's transl)].
    Le Merrer M, Briard ML, Demenais F, Feingold J, Frézal J.
    Arch Fr Pediatr; 1980 Oct; 37(8):521-5. PubMed ID: 7004382
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  • 20. Family studies on HLA system in children with CNS malformations.
    Pietrzyk JJ, Turowski G.
    Indian J Exp Biol; 1980 Mar; 18(3):278-82. PubMed ID: 6993348
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