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Journal Abstract Search

459 related items for PubMed ID: 16810710

  • 41. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
    [Abstract] [Full Text] [Related]

  • 42. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
    [Abstract] [Full Text] [Related]

  • 43. Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
    Neiswanger K, Hohler PM, Hively-Thomas LB, McPherson EW, Hogge WA, Surti U.
    Prenat Diagn; 2006 May 05; 26(5):454-61. PubMed ID: 16557642
    [Abstract] [Full Text] [Related]

  • 44. Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells.
    Tsai MC, Cheng HY, Su MT, Chen M, Kuo PL.
    Taiwan J Obstet Gynecol; 2014 Dec 05; 53(4):598-601. PubMed ID: 25510708
    [Abstract] [Full Text] [Related]

  • 45. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
    Slater HR, Vaux C, Pertile M, Burgess T, Petrovic V.
    Prenat Diagn; 1997 Feb 05; 17(2):109-13. PubMed ID: 9061757
    [Abstract] [Full Text] [Related]

  • 46. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.
    Chen CP, Chang SJ, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Aug 05; 55(4):602-3. PubMed ID: 27590391
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  • 49. Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Wu CY, Chern SR, Chen SW, Wu FT, Chen WL, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jul 05; 59(4):604-606. PubMed ID: 32653138
    [Abstract] [Full Text] [Related]

  • 50. Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin.
    Paulyson KJ, Sherer DM, Christian SL, Lewis KM, Ledbetter DH, Salafia CM, Meck JM.
    Prenat Diagn; 1996 Nov 05; 16(11):1021-6. PubMed ID: 8953635
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  • 51. The association between preeclampsia and placental trisomy 16 mosaicism.
    Yong PJ, Langlois S, von Dadelszen P, Robinson W.
    Prenat Diagn; 2006 Oct 05; 26(10):956-61. PubMed ID: 16874839
    [Abstract] [Full Text] [Related]

  • 52. Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Hsieh CE, Chern SR, Chen SW, Wu FT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2021 May 05; 60(3):540-542. PubMed ID: 33966744
    [Abstract] [Full Text] [Related]

  • 53. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May 05; 25(5):354-7. PubMed ID: 15906424
    [Abstract] [Full Text] [Related]

  • 54. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
    Chen CP, Su YN, Hsu CY, Chern SR, Lee CC, Chen YT, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec 05; 50(4):485-91. PubMed ID: 22212322
    [Abstract] [Full Text] [Related]

  • 55. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.
    Pediatr Dermatol; 2004 Dec 05; 21(6):636-41. PubMed ID: 15575846
    [Abstract] [Full Text] [Related]

  • 56. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.
    Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Pan CW, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Apr 05; 56(2):238-242. PubMed ID: 28420516
    [Abstract] [Full Text] [Related]

  • 57. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.
    J Perinatol; 1998 Apr 05; 18(5):395-8. PubMed ID: 9766419
    [Abstract] [Full Text] [Related]

  • 58. Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.
    Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD.
    Am J Med Genet; 1996 Nov 11; 65(4):348-52. PubMed ID: 8923948
    [Abstract] [Full Text] [Related]

  • 59. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
    Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P.
    Prenat Diagn; 1997 Mar 11; 17(3):201-42. PubMed ID: 9110367
    [Abstract] [Full Text] [Related]

  • 60. Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.
    Spiro R, Rita D, Jazmines L, Jones C, Booth CW.
    Prenat Diagn; 1996 Aug 11; 16(8):734-40. PubMed ID: 8878284
    [Abstract] [Full Text] [Related]

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