These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

228 related items for PubMed ID: 8878286

  • 41. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
    [Abstract] [Full Text] [Related]

  • 42. Molecular-cytogenetic investigations of ten term placentae in cases of prenatally diagnosed mosaicism.
    Schubert R, Raff R, Schwanitz G.
    Prenat Diagn; 1996 Oct; 16(10):907-13. PubMed ID: 8938059
    [Abstract] [Full Text] [Related]

  • 43. Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns.
    Pletcher BA, Sanz MM, Schlessel JS, Kunaporn S, McKenna C, Bialer MG, Alonso ML, Zaslav AL, Brown WT, Ray JH.
    Prenat Diagn; 1994 Oct; 14(10):933-40. PubMed ID: 7899268
    [Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49. A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.
    Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK.
    Prenat Diagn; 1996 Apr; 16(4):371-4. PubMed ID: 8734817
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation.
    Webb AL, Sturgiss S, Warwicker P, Robson SC, Goodship JA, Wolstenholme J.
    Prenat Diagn; 1996 Oct; 16(10):958-62. PubMed ID: 8938070
    [Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. A retrospective evaluation of maternal serum screening for the detection of fetal aneuploidy.
    Suzumori K, Tanemura M, Murakami I, Okada S, Natori M, Tanaka M, Takagi T, Sato A.
    Prenat Diagn; 1997 Sep; 17(9):861-6. PubMed ID: 9316131
    [Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. Case of non-mosaic trisomy 20 in amniotic fluid cultures without anomalies in the fetus: cytogenetic discrepancy between amniocytes and fetal blood.
    Maeda K, Imoto I, Kaji T, Yoshida Y, Nakayama S, Irahara M.
    J Obstet Gynaecol Res; 2015 Jan; 41(1):141-4. PubMed ID: 25164874
    [Abstract] [Full Text] [Related]

  • 59. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R, Pfeiffer RA, Kollert A, Beinder E.
    Z Geburtshilfe Neonatol; 2000 Jan; 204(1):1-7. PubMed ID: 10721179
    [Abstract] [Full Text] [Related]

  • 60. Human chorionic gonadotrophin and trisomy 18.
    Barkai G, Chaki R, Sochat M, Goldman B.
    Am J Med Genet; 1991 Oct 01; 41(1):52-3. PubMed ID: 1719814
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.