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Journal Abstract Search

252 related items for PubMed ID: 30204977

  • 1. DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE.
    Attig A, Ben Jemaa L, Kraoua L, Jilani H, Maazoul F, Mrad R.
    Genet Couns; 2016; 27(3):441-446. PubMed ID: 30204977
    [No Abstract] [Full Text] [Related]

  • 2. Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.
    Tucker T, Steinraths M, Oh T, Nelson TN, Van Allen MI, Brown L, Schlade-Bartusiak K.
    Clin Dysmorphol; 2016 Apr; 25(2):77-81. PubMed ID: 26636500
    [No Abstract] [Full Text] [Related]

  • 3. Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.
    Sun S, Zhan F, Jiang J, Zhang X, Yan L, Cai W, Liu H, Cao D.
    BMC Med Genomics; 2019 Dec 21; 12(1):197. PubMed ID: 31864361
    [Abstract] [Full Text] [Related]

  • 4. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC, Sünnetçi D, Cine N, Savli H, Okten A, Açikgöz EG, Sönmez FM.
    Genet Couns; 2014 Dec 21; 25(3):305-13. PubMed ID: 25365853
    [Abstract] [Full Text] [Related]

  • 5. Fetal trisomy 8 mosaicism associated with truncus arteriosus Type I.
    Sherer DM, Dalloul M, Pinard V, Sheu J, Abulafia O.
    Ultrasound Obstet Gynecol; 2017 Oct 21; 50(4):541-542. PubMed ID: 28093816
    [No Abstract] [Full Text] [Related]

  • 6. Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis.
    Altıner Ş, Kutlay NY, İlhan O.
    Cytogenet Genome Res; 2016 Oct 21; 150(1):35-39. PubMed ID: 27838684
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  • 12. Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney.
    Aykut A, Cogulu O, Ozkinay F.
    Genet Couns; 2012 Oct 21; 23(1):77-80. PubMed ID: 22611646
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  • 15. 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 21; 27():38-42. PubMed ID: 28697408
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  • 17. Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.
    Yao H, Zhang L, Zhang H, Jiang F, Hu H, Chen F, Jiang H, Mu F, Zhao L, Liang Z, Wang W.
    Prenat Diagn; 2012 Nov 21; 32(11):1114-6. PubMed ID: 22903289
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  • 18. Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis.
    Sifakis S, Anagnostopoulou K, Plastira K, Vrachnis N, Konstantinidou A, Sklavounou E.
    Birth Defects Res A Clin Mol Teratol; 2012 Apr 21; 94(4):245-8. PubMed ID: 22282126
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  • 19. [Child language development delay in craniofacial dysplasia].
    Schwemmle C, Lüerssen K, Tolloczko R, Ptok M.
    HNO; 2004 Feb 21; 52(2):150-2. PubMed ID: 14968319
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