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Journal Abstract Search

123 related items for PubMed ID: 3303006

  • 1. Incidence of fetal chromosome abnormalities in 2264 low-risk women.
    Tabor A, Philip J.
    Prenat Diagn; 1987 Jun; 7(5):355-62. PubMed ID: 3303006
    [Abstract] [Full Text] [Related]

  • 2. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases.
    Yaegashi N, Senoo M, Uehara S, Suzuki H, Maeda T, Fujimori K, Hirahara F, Yajima A.
    J Hum Genet; 1998 Jun; 43(2):85-90. PubMed ID: 9621511
    [Abstract] [Full Text] [Related]

  • 3. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J, Chen L, Zhou C, Wang L, Xie H, Xiao Y, Zhu H, Hu T, Zhang Z, Zhu Q, Liu Z, Liu S, Wang H, Xu M, Ren Z, Yu F, Cram DS, Liu H.
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [Abstract] [Full Text] [Related]

  • 4. Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981.
    Stene J, Stene E, Mikkelsen M.
    Prenat Diagn; 1984 Sep; 4 Spec No():81-95. PubMed ID: 6235486
    [Abstract] [Full Text] [Related]

  • 5. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic results from the U.S. Collaborative Study on CVS.
    Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L, Mahoney MJ, Desnick RJ, Schulman J, Copeland KL.
    Prenat Diagn; 1992 May; 12(5):317-45. PubMed ID: 1523201
    [Abstract] [Full Text] [Related]

  • 7. A multicenter study of fetal chromosomal abnormalities in Chinese women of advanced maternal age.
    Zhu Y, Lu S, Bian X, Wang H, Zhu B, Wang H, Xu Z, Xu L, Yan W, Zeng Y, Chen Z, Tang S, Shen G, Miao Z.
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):379-84. PubMed ID: 27343319
    [Abstract] [Full Text] [Related]

  • 8. [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 Jun; 204(1):1-7. PubMed ID: 10721179
    [Abstract] [Full Text] [Related]

  • 9. Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory.
    Caron L, Tihy F, Dallaire L.
    Am J Med Genet; 1999 Jan 15; 82(2):149-54. PubMed ID: 9934980
    [Abstract] [Full Text] [Related]

  • 10. Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, parental-age associations, sex-ratio trends, and comparisons with rates of mutants.
    Hook EB, Schreinemachers DM, Willey AM, Cross PK.
    Am J Hum Genet; 1984 Mar 15; 36(2):422-43. PubMed ID: 6711562
    [Abstract] [Full Text] [Related]

  • 11. Comparison of multiple-marker screening with amniocentesis for the detection of fetal aneuploidy in women > or = 35 years old.
    Wenstrom KD, Desai R, Owen J, DuBard MB, Boots L.
    Am J Obstet Gynecol; 1995 Oct 15; 173(4):1287-92. PubMed ID: 7485339
    [Abstract] [Full Text] [Related]

  • 12. Fetal karyotyping for chromosome abnormalities after an unexplained elevated maternal serum alpha-fetoprotein screening.
    Feuchtbaum LB, Cunningham G, Waller DK, Lustig LS, Tompkinson DG, Hook EB.
    Obstet Gynecol; 1995 Aug 15; 86(2):248-54. PubMed ID: 7542378
    [Abstract] [Full Text] [Related]

  • 13. Ultrasound-adjusted risk and spectrum of fetal chromosomal abnormality in women with elevated maternal serum alpha-fetoprotein.
    Megerian G, Godmilow L, Donnenfeld AE.
    Obstet Gynecol; 1995 Jun 15; 85(6):952-6. PubMed ID: 7539525
    [Abstract] [Full Text] [Related]

  • 14. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.
    Prenat Diagn; 1996 Jan 15; 16(1):1-28. PubMed ID: 8821848
    [Abstract] [Full Text] [Related]

  • 15. Noninvasive prenatal testing for whole fetal chromosomal aneuploidies: a multicenter prospective cohort trial in Taiwan.
    Shaw SW, Hsiao CH, Chen CY, Ren Y, Tian F, Tsai C, Chen M, Cheng PJ.
    Fetal Diagn Ther; 2014 Jan 15; 35(1):13-7. PubMed ID: 24296685
    [Abstract] [Full Text] [Related]

  • 16. Fetal chromosome analysis: screening for chromosome disease?
    Philip J, Tabor A, Bang J, Madsen M.
    Prenat Diagn; 1983 Jul 15; 3(3):209-18. PubMed ID: 6622404
    [Abstract] [Full Text] [Related]

  • 17. Chromosome findings in 2,500 second trimester amniocenteses.
    Crandall BF, Lebherz TB, Rubinstein L, Robertson RD, Sample WF, Sarti D, Howard J.
    Am J Med Genet; 1980 Jul 15; 5(4):345-56. PubMed ID: 6446858
    [Abstract] [Full Text] [Related]

  • 18. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
    Peng HH, Chao AS, Wang TH, Chang YL, Chang SD.
    J Reprod Med; 2006 Sep 15; 51(9):699-703. PubMed ID: 17039698
    [Abstract] [Full Text] [Related]

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  • 20. Temporal changes in Ohio amniocentesis utilization during the first twelve years (1972-1983), and frequency of chromosome abnormalities observed.
    Naber JM, Huether CA, Goodwin BA.
    Prenat Diagn; 1987 Sep 15; 7(1):51-65. PubMed ID: 2950387
    [Abstract] [Full Text] [Related]

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