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Journal Abstract Search

166 related items for PubMed ID: 26384070

  • 1. Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result.
    Chen CP, Lin SP, Li HB, Chen YN, Wang W.
    Taiwan J Obstet Gynecol; 2015 Aug; 54(4):450-1. PubMed ID: 26384070
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  • 2. TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION.
    Atik T, Karaca E, Ozkinay E, Cogulu O.
    Genet Couns; 2015 Aug; 26(4):431-5. PubMed ID: 26852514
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  • 3. First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.
    Guterman S, Hervé B, Rivière J, Fauvert D, Clement P, Vialard F.
    J Obstet Gynaecol Res; 2018 Mar; 44(3):570-575. PubMed ID: 29160022
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  • 6. Kleefstra Syndrome: The First Case Report From Iran.
    Noruzinia M, Ahmadvand M, Bashti O, Salehi Chaleshtori AR.
    Acta Med Iran; 2017 Oct; 55(10):650-654. PubMed ID: 29228531
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  • 10. Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact.
    Hervé B, Roume J, Cognard S, Fauvert D, Molina-Gomes D, Vialard F.
    Eur J Med Genet; 2015 Oct; 58(6-7):346-50. PubMed ID: 25963108
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  • 12. [Prenatal genetic diagnosis for a fetus with atypical neurofibromatosis type 1 microdeletion].
    Lin S, Wu J, Zhang Z, Ji Y, Fang Q, Chen B, Luo Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):212-5. PubMed ID: 27060318
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  • 13. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry.
    Chen CP, Hwang KS, Su HY, Lin SP, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):125-8. PubMed ID: 23548233
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  • 14. A patient with 9q subtelomeric deletion syndrome with additional findings.
    Tug E, Cavdarli B, Karaoguz MY, Percin FE.
    Genet Couns; 2012 Mar; 23(4):465-71. PubMed ID: 23431745
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  • 15. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
    Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W.
    Gene; 2013 Dec 10; 532(1):80-6. PubMed ID: 24055486
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  • 16. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
    Chen CP, Su YN, Lin SP, Chern SR, Su JW, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar 10; 52(1):120-4. PubMed ID: 23548232
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  • 19. False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism.
    Gao Y, Stejskal D, Jiang F, Wang W.
    Ultrasound Obstet Gynecol; 2014 Apr 10; 43(4):477-8. PubMed ID: 24186002
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