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Journal Abstract Search

147 related items for PubMed ID: 11146460

  • 21.
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  • 23. First-trimester sonographic findings associated with a Dandy-Walker malformation and inferior vermian hypoplasia.
    Bornstein E, Goncalves Rodríguez JL, Álvarez Pavón EC, Quiroga H, Or D, Divon MY.
    J Ultrasound Med; 2013 Oct; 32(10):1863-8. PubMed ID: 24065268
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  • 24. Dandy-Walker malformation complex: correlation between ultrasonographic diagnosis and postmortem neuropathology.
    Phillips JJ, Mahony BS, Siebert JR, Lalani T, Fligner CL, Kapur RP.
    Obstet Gynecol; 2006 Mar; 107(3):685-93. PubMed ID: 16507942
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  • 26. [Apropos of a case of Dandy-Walker syndrome associated with chromosome abnormalities].
    Patacchiola F, Carta G, Iovenitti P, Bonitatibus A, Mascaretti G, Caserta D, Moscarini M.
    Minerva Ginecol; 1999 Mar; 51(3):95-8. PubMed ID: 10352541
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  • 28. A case of a Dandy-Walker variant: the importance of a multidisciplinary team approach using complementary techniques to obtain accurate diagnostic information.
    Lavanya T, Cohen M, Gandhi SV, Farrell T, Whitby EH.
    Br J Radiol; 2008 Oct; 81(970):e242-5. PubMed ID: 18796551
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  • 29. Rotation of the vermis as a cause of enlarged cisterna magna on prenatal imaging.
    Zalel Y, Gilboa Y, Gabis L, Ben-Sira L, Hoffman C, Wiener Y, Achiron R.
    Ultrasound Obstet Gynecol; 2006 May; 27(5):490-3. PubMed ID: 16619381
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  • 31. Dandy-Walker variant: prenatal sonographic features and clinical outcome.
    Estroff JA, Scott MR, Benacerraf BR.
    Radiology; 1992 Dec; 185(3):755-8. PubMed ID: 1438757
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  • 32. FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
    Aldinger KA, Lehmann OJ, Hudgins L, Chizhikov VV, Bassuk AG, Ades LC, Krantz ID, Dobyns WB, Millen KJ.
    Nat Genet; 2009 Sep; 41(9):1037-42. PubMed ID: 19668217
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  • 35. Normal and abnormal anatomy of the cerebellar vermis in midgestational human fetuses.
    Kapur RP, Mahony BS, Finch L, Siebert JR.
    Birth Defects Res A Clin Mol Teratol; 2009 Aug; 85(8):700-9. PubMed ID: 19441098
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  • 37. MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.
    Gorukmez O, Gorukmez O, Sag OS, Yakut T, Gulten T.
    Genet Couns; 2015 Aug; 26(2):163-9. PubMed ID: 26349185
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  • 38. An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) mother.
    Neu RL, Dennis NR, Lanman JT, Bannerman RM.
    Ann Genet; 1979 Aug; 22(3):151-4. PubMed ID: 316670
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  • 40. Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3).
    Vundinti BR, Kerketta L, Korgaonkar S, Ghosh K.
    Indian J Hum Genet; 2007 Jan; 13(1):33-5. PubMed ID: 21957340
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