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Journal Abstract Search

133 related items for PubMed ID: 24812702

  • 1. Intracranial teratoma in children: the role of chromosome 21 trisomy.
    Ferraz ST, Valera ET, Brassesco MS, Santos de Oliveira R, Carlos dos Santos A, Saggioro FP, Neder L, Scrideli CA, Tone LG.
    Neuropathology; 2014 Apr; 34(2):197-200. PubMed ID: 24812702
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  • 3. Monosomy 22 in rhabdoid or atypical tumors of the brain.
    Biegel JA, Rorke LB, Packer RJ, Emanuel BS.
    J Neurosurg; 1990 Nov; 73(5):710-4. PubMed ID: 2213160
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  • 6. The origin of extragonadal teratoma: case report of an immature teratoma occurring in a prenatal brain.
    Saiga T, Osasa H, Hatayama H, Miyamoto T, Ono H, Mikami T.
    Pediatr Pathol; 1991 Nov; 11(5):759-70. PubMed ID: 1660602
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  • 7. Infratentorial immature teratoma of congenital origin can be associated with a 20-year survival outcome: a case report and review of literature.
    Maghrabi Y, Kurdi ME, Baeesa SS.
    World J Surg Oncol; 2019 Jan 19; 17(1):22. PubMed ID: 30660187
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  • 8. Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype-phenotype association.
    Pelleri MC, Locatelli C, Mattina T, Bonaglia MC, Piazza F, Magini P, Antonaros F, Ramacieri G, Vione B, Vitale L, Seri M, Strippoli P, Cocchi G, Piovesan A, Caracausi M.
    BMC Med Genomics; 2022 Dec 21; 15(1):266. PubMed ID: 36544206
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  • 9. Intracranial germ cell tumour (embryonal carcinoma with teratoma) with complex karyotype including isochromosome 12p.
    Losi L, Polito P, Hagemeijer A, Buonamici L, Van den Berghe H, Dal Cin P.
    Virchows Arch; 1998 Dec 21; 433(6):571-4. PubMed ID: 9870692
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  • 10. A Down syndrome female infant with partial trisomy of chromosome 21--abnormal nuchal translucency screening test.
    Strah D, Veble A, Rudolf G, Writzl K, Gersak K.
    Genet Couns; 2008 Dec 21; 19(4):429-32. PubMed ID: 19239088
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  • 14. Adenocarcinoma arising from intracranial recurrent mature teratoma and featuring mutated KRAS and wild-type BRAF genes.
    Kim ES, Kwon MJ, Song JH, Kim DH, Park HR.
    Neuropathology; 2015 Feb 21; 35(1):44-9. PubMed ID: 25039399
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  • 15. Atypical Down syndrome phenotype with severe developmental delay, hypertonia, and seizures in a child with translocation trisomy 21.
    Keppler-Noreuil KM, Welch JL, Major HJ, Qiau Q, Jordan DK, Patil SR.
    Dev Med Child Neurol; 2002 Jan 21; 44(1):64-7. PubMed ID: 11811653
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  • 16. Trisomy 12 and translocation (7;9) in an ovarian immature teratoma.
    López Ginés C, Gil R, Pellin A, Martorell M, Vilar F, Llombart-Bosch A.
    Int J Gynecol Pathol; 1989 Jan 21; 8(3):277-85. PubMed ID: 2767876
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  • 17. Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian population.
    Mandava S, Koppaka N, Bhatia V, Das BR.
    Genet Test Mol Biomarkers; 2010 Aug 21; 14(4):499-504. PubMed ID: 20642367
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  • 18. AN INTERCHANGE TRISOMY RESULTED IN DOWN SYNDROME.
    Tug E, Karaoguz MY, Bakir A.
    Genet Couns; 2016 Aug 21; 27(3):429-431. PubMed ID: 30204975
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  • 20. A patient with Down syndrome with a de novo derivative chromosome 21.
    Cetin Z, Yakut S, Mihci E, Manguoglu AE, Berker S, Keser I, Luleci G.
    Gene; 2012 Oct 10; 507(2):159-64. PubMed ID: 22827956
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