These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 18564502)

  • 1. A male case with double aneuploidy (48,XXY,+21).
    Akbas E; Soylemez F; Savasoglu K; Halliogluand O; Balci S
    Genet Couns; 2008; 19(1):59-63. PubMed ID: 18564502
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Double aneuploidy in a Turkish child: Down-Klinefelter syndrome.
    Karaman A; Kabalar E
    Congenit Anom (Kyoto); 2008 Mar; 48(1):45-7. PubMed ID: 18230121
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Double trisomy (48,XXY,+21) in monozygotic twins: case report and review of the literature.
    Iliopoulos D; Poultsides G; Peristeri V; Kouri G; Andreou A; Voyiatzis N
    Ann Genet; 2004; 47(1):95-8. PubMed ID: 15050879
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
    Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Double aneuploidy with Down's-Klinefelter's syndrome.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Apr; 95(4):350-2. PubMed ID: 8935309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Developmental consequences of autosomal aneuploidy in mammals.
    Gearhart JD; Oster-Granite ML; Reeves RH; Coyle JT
    Dev Genet; 1987; 8(4):249-65. PubMed ID: 2971493
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Case of double aneuploidy: trisomy 18 and XXY].
    Bach C; Toublanc JE; Gautier M
    Ann Genet; 1973 Mar; 16(1):61-6. PubMed ID: 4541812
    [No Abstract]   [Full Text] [Related]  

  • 9. Double aneuploidy: the frequency of XXY in males with Down's syndrome.
    Hecht F; Nievaard JE; Duncanson N; Miller JR; Higgins JV; Kimberling WJ; Walker FA; Smith GS; Thuline HC; Tischler B
    Am J Hum Genet; 1969 Jul; 21(4):352-9. PubMed ID: 4240108
    [No Abstract]   [Full Text] [Related]  

  • 10. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular biology usefulness for rapid diagnosis of Down's syndrome and common aneuploidies].
    Fauret AL; Bilan F; Patri S; Couet D; Marechaud M; Pierre F; Gilbert-Dussardier B; Kitzis A
    Gynecol Obstet Fertil; 2009; 37(7-8):611-9. PubMed ID: 19574080
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Double Trisomy 48,XXY,+21 in a Neonate with Congenital Heart Disease.
    Bijanzadeh M; Rajaei Behbahani S
    Arch Iran Med; 2020 May; 23(5):356-358. PubMed ID: 32383621
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+21.
    Costa GRC; Jorente J; Pontes LB; Viguetti Campos NL; Marques-de-Faria AP; Vieira TP; Steiner CE
    Cytogenet Genome Res; 2024; 164(2):103-109. PubMed ID: 39068925
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mosaic trisomy 21/monosomy 21 in a living female infant.
    Nguyen HP; Riess A; Krüger M; Bauer P; Singer S; Schneider M; Enders H; Dufke A
    Cytogenet Genome Res; 2009; 125(1):26-32. PubMed ID: 19617693
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases].
    Castel Y; Le Marec B; Toudic L; Lemarchand M; Cosson JP
    Pediatrie; 1983 Jun; 38(4):235-41. PubMed ID: 6225989
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A male phenotype with Aicardi syndrome.
    Zubairi MS; Carter RF; Ronen GM
    J Child Neurol; 2009 Feb; 24(2):204-7. PubMed ID: 19182158
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 14(4):499-504. PubMed ID: 20642367
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes.
    Kovaleva NV; Mutton DE
    Am J Med Genet A; 2005 Apr; 134A(1):24-32. PubMed ID: 15704133
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An infant with Down-Turner double aneuploidy: a case report and literature review.
    Jaruratanasirikul S; Jinorose U
    J Med Assoc Thai; 1995 Feb; 78(2):108-12. PubMed ID: 7629445
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Double aneuploidy in spontaneous miscarriages: two case reports and review of the literature.
    Korucuoglu U; Erdem M; Pala E; Karaoguz MY; Erdem A; Biri A
    Fetal Diagn Ther; 2008; 24(2):106-10. PubMed ID: 18648209
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.