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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

226 related items for PubMed ID: 16491370

  • 21.
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  • 22. Nuchal thickening in Jacobsen syndrome.
    McClelland SM, Smith AP, Smith NC, Gray ES, Diack JS, Dean JC.
    Ultrasound Obstet Gynecol; 1998 Oct; 12(4):280-2. PubMed ID: 9819862
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  • 24. PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW.
    Puvabanditsin S, Herrera-Garcia G, Gengel N, Hussein K, February M, Mayne J, Mehta R.
    Genet Couns; 2016 Oct; 27(1):35-41. PubMed ID: 27192890
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  • 29. Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities.
    Widschwendter A, Riha K, Duba HC, Kreczy A, Marth C, Schwärzler P.
    Ultrasound Obstet Gynecol; 2002 Apr; 19(4):396-9. PubMed ID: 11952971
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  • 32. Inverted duplication of the distal short arm of chromosome 3 associated with lobar holoprosencephaly and lumbosacral meningomyelocele.
    Kennedy D, Silver MM, Winsor EJ, Toi A, Provias J, Macha M, Precht K, Ledbetter DH, Chitayat D.
    Am J Med Genet; 2000 Mar 20; 91(3):167-70. PubMed ID: 10756335
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  • 33. Prenatal detection of associated anomalies in fetuses diagnosed with cleft lip with or without cleft palate in utero.
    Chmait R, Pretorius D, Moore T, Hull A, James G, Nelson T, Jones M.
    Ultrasound Obstet Gynecol; 2006 Feb 20; 27(2):173-6. PubMed ID: 16247756
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  • 34. Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.
    Uwineza A, Pierquin G, Gaillez S, Jamar M, Hellin AC, Caberg JH, Bours V.
    Genet Couns; 2013 Feb 20; 24(2):193-200. PubMed ID: 24032290
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  • 35. Prenatal diagnosis of Aicardi-Goutières syndrome.
    Le Garrec M, Doret M, Pasquier JC, Till M, Lebon P, Buenerd A, Escalon J, Gaucherand P.
    Prenat Diagn; 2005 Jan 20; 25(1):28-30. PubMed ID: 15662687
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  • 38. Distal 13q monosomy and neural tube defects.
    Lurie IW, Novikova IV, Tarletskaya OA, Lazarevich AA, Gromyko OA.
    Genet Couns; 2016 Jan 20; 27(2):177-86. PubMed ID: 29485808
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  • 39. Prenatal sonographic diagnosis of Malpuech syndrome.
    Turnbull C, Lees M, Chitty LS.
    Prenat Diagn; 2006 Dec 20; 26(12):1121-3. PubMed ID: 17019743
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  • 40. Prenatal diagnosis of Smith-Lemli-Opitz syndrome, type II.
    Johnson JA, Aughton DJ, Comstock CH, von Oeyen PT, Higgins JV, Schulz R.
    Am J Med Genet; 1994 Jan 15; 49(2):240-3. PubMed ID: 8116676
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