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Journal Abstract Search

252 related items for PubMed ID: 30204977

  • 41.
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  • 43. Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome.
    McGaughran J, Aftimos S, Oei P.
    Am J Med Genet; 2000 Oct 02; 94(4):311-5. PubMed ID: 11038445
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  • 45. A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin.
    McGregor-Schuerman M, Lo Fo Sang A, Bihari S, Ramdajal N, Suijkerbuijk RF, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2020 Jun 02; 63(6):103922. PubMed ID: 32240827
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  • 47. 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 02; 170(11):2870-2881. PubMed ID: 27644018
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  • 48. 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 02; 43(4):477-8. PubMed ID: 24186002
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  • 49.
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  • 50. Prenatal diagnosis of trisomy 8 mosaicism.
    Chen CP, Su YN, Chern SR, Chen YT, Su JW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2012 Dec 02; 51(4):666-8. PubMed ID: 23276580
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  • 51. Trisomy 8 mosaicism and favorable outcome after treatment of infantile spasms: case report.
    Datta A, Picker J, Rotenberg A.
    J Child Neurol; 2010 Oct 02; 25(10):1275-7. PubMed ID: 20489041
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  • 52. Confined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer.
    Valind A, Pal N, Asmundsson J, Gisselsson D, Holmquist Mengelbier L.
    Genes Chromosomes Cancer; 2014 Jul 02; 53(7):634-8. PubMed ID: 24729308
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  • 55. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
    Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Oct 02; 56(5):691-693. PubMed ID: 29037560
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  • 56. Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia.
    Fryns JP, Devriendt K, Detroch C, Decock P.
    Genet Couns; 1998 Oct 02; 9(1):51-4. PubMed ID: 9555588
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  • 58. [Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype].
    Pachajoa H.
    Arch Argent Pediatr; 2013 Oct 02; 111(4):e101-4. PubMed ID: 23912296
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  • 59.
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  • 60. Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome.
    Welsh C, Khalili S, Hazrati LN, Mireskandari K.
    Cornea; 2018 Dec 02; 37(12):1596-1600. PubMed ID: 30272617
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