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 *

139 related articles for article (PubMed ID: 7629445)

  • 21. Supernumerary chromosomes in mosaic Turner syndrome.
    Thong MK; Manonmani V; Norlasiah IS
    Med J Malaysia; 1996 Dec; 51(4):487-90. PubMed ID: 10968041
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Tetrasomy 21 transient leukemia with a GATA1 mutation in a phenotypically normal trisomy 21 mosaic infant: case report and review of the literature.
    Sandoval C; Pine SR; Guo Q; Sastry S; Stewart J; Kronn D; Jayabose S
    Pediatr Blood Cancer; 2005 Jan; 44(1):85-91. PubMed ID: 15390279
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dysgerminoma in a pure 45,X Turner syndrome: report of a case and review of the literature.
    Pierga JY; Giacchetti S; Vilain E; Extra JM; Brice P; Espie M; Maragi JA; Fellous M; Marty M
    Gynecol Oncol; 1994 Dec; 55(3 Pt 1):459-64. PubMed ID: 7835789
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. [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]  

  • 26. 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]  

  • 27. 45,X/46,XX mosaicism in a mother and one of her discordant monozygotic twin daughters: report of one case.
    Su PH; Chen JY; Chen SJ; Hung HM; Ting HC; Lin CY; Quek YW
    Acta Paediatr Taiwan; 2006; 47(5):252-4. PubMed ID: 17352314
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of trisomy 21 and X/XX sex chromosome mosaicism.
    McCorquodale MM; Cummins T; Furlong J
    Prenat Diagn; 1985; 5(4):295-8. PubMed ID: 2931678
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Turner syndrome with complex mosaic monosomy and structural aorta anomalies.
    Tissières P; Didier D; Dahoun S; Jaeggi ET
    J Pediatr; 2003 Mar; 142(3):341. PubMed ID: 12640386
    [No Abstract]   [Full Text] [Related]  

  • 30. [Turner syndrome: mosaic and isochromosome q in a young African woman].
    Mensah-Ado I; Lauhbouet MD; Lokrou A; Ehouman A; Morlier G
    Med Trop (Mars); 1994; 54(4):349-51. PubMed ID: 7746129
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Down syndrome with XO/XX mosaicism.
    Bajnóczky K; Méhes K
    Acta Paediatr Acad Sci Hung; 1979; 20(2-3):237-9. PubMed ID: 161847
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 45,X/47,XX, + 18 constitutional mosaicism: clinical presentation and evidence for a somatic origin of the aneuploid cell lines.
    Genuardi M; Pomponi MG; Torrisi L; Neri G; Stagni ML; Tozzi C
    J Med Genet; 1999 Jun; 36(6):496-8. PubMed ID: 10874643
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. Free beta hCG screening of hydropic and non-hydropic Turner syndrome pregnancies.
    Laundon CH; Spencer K; Macri JN; Anderson RW; Buchanan PD
    Prenat Diagn; 1996 Sep; 16(9):853-6. PubMed ID: 8905900
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mosaicism for trisomy 21 in a patient with young-onset dementia: a case report and brief literature review.
    Ringman JM; Rao PN; Lu PH; Cederbaum S
    Arch Neurol; 2008 Mar; 65(3):412-5. PubMed ID: 18332257
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Low-level hyperinsulinism with hypoglycemic spells in an infant with mosaic Turner syndrome and mild Kabuki-like phenotype: a case report and review of the literature.
    Pietzner V; Weigel JF; Wand D; Merkenschlager A; Bernhard MK
    J Pediatr Endocrinol Metab; 2014 Jan; 27(1-2):165-70. PubMed ID: 23950569
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Detection of aneuploidies using in situ hybridization in cells of the oral mucosa].
    Frías S; Ordaz G; Blanco B; Molina B; del Castillo V; Carnevale A
    Rev Invest Clin; 1996; 48(5):355-60. PubMed ID: 9005512
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cryopreservation of ovarian tissue and in vitro matured oocytes in a female with mosaic Turner syndrome: Case Report.
    Huang JY; Tulandi T; Holzer H; Lau NM; Macdonald S; Tan SL; Chian RC
    Hum Reprod; 2008 Feb; 23(2):336-9. PubMed ID: 18056118
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Cryptic mosaicism for monosomy 20 identified in renal tract cells.
    Stefanou EG; Crocker M; Boon A; Stewart H
    Clin Genet; 2006 Sep; 70(3):228-32. PubMed ID: 16922725
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.