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Journal Abstract Search

326 related items for PubMed ID: 28697408

  • 1. A finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestations.
    Yang X, Ye Z, Zhang X, Wang H, Liu C.
    Leg Med (Tokyo); 2017 Jul; 27():38-42. PubMed ID: 28697408
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  • 5. A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.
    Li J, Xie M, Wang F, Ma J, Li J, Chen C, Li Z, Wang J, Zhang Y, Li Y.
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1279. PubMed ID: 32463164
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  • 6. Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.
    Wigby K, D'Epagnier C, Howell S, Reicks A, Wilson R, Cordeiro L, Tartaglia N.
    Am J Med Genet A; 2016 Nov; 170(11):2870-2881. PubMed ID: 27644018
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  • 7. Triple X syndrome.
    Afshan A.
    J Pak Med Assoc; 2012 Apr; 62(4):392-4. PubMed ID: 22755288
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  • 8. A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the Literature.
    Mavridi A, Ntali G, Theodora M, Stamatelopoulos K, Michala L.
    J Pediatr Adolesc Gynecol; 2018 Dec; 31(6):651-654. PubMed ID: 30012427
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  • 10. Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX.
    Cremonini G, Poggi A, Capucci R, Vesce F, Patella A, Marci R.
    J Obstet Gynaecol Res; 2014 Jan; 40(1):259-62. PubMed ID: 23937348
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  • 13. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
    Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AM.
    Am J Obstet Gynecol; 2017 Dec; 217(6):691.e1-691.e6. PubMed ID: 29032050
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  • 15. Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia.
    Sharapova SO, Valochnik AV, Guryanova IE, Sakovich IS, Aleinikova OV.
    Immunogenetics; 2018 Sep; 70(9):613-617. PubMed ID: 29492593
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  • 16. Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
    Zhang B, Lu BY, Yu B, Zheng FX, Zhou Q, Chen YP, Zhang XQ.
    J Int Med Res; 2017 Apr; 45(2):621-630. PubMed ID: 28357876
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  • 17. [Gonosomal trisomy syndrome. Five case reports and review of literature].
    Schwemmle C, Jungheim M, Ptok M.
    Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211
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  • 18. Fetal axillary cystic hygroma: a novel association with triple X syndrome.
    Iskender C, Tarım E, Cok T, Yalcinkaya C, Kalaycı H, Sahin F.
    Birth Defects Res A Clin Mol Teratol; 2012 Nov; 94(11):955-7. PubMed ID: 23109196
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  • 19. Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.
    Viuff MH, Stochholm K, Uldbjerg N, Nielsen BB, Danish Fetal Medicine Study Group, Gravholt CH.
    Hum Reprod; 2015 Oct; 30(10):2419-26. PubMed ID: 26251461
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  • 20. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome.
    Sharma R, Harris VM, Cavett J, Kurien BT, Liu K, Koelsch KA, Fayaaz A, Chaudhari KS, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Alarcón-Riquelme M, Mariette X, Lessard CJ, Harley JB, Ng WF, Rasmussen A, Sivils KL, Scofield RH.
    Arthritis Rheumatol; 2017 Nov; 69(11):2187-2192. PubMed ID: 28692793
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