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 *

659 related articles for article (PubMed ID: 9412788)

  • 1. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B
    Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.
    Ginsburg C; Fokstuen S; Schinzel A
    Am J Med Genet; 2000 Dec; 95(5):454-60. PubMed ID: 11146466
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M; Wethling H; Niemeyer ML; Schwinger E
    Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.
    Papenhausen PR; Mueller OT; Johnson VP; Sutcliffe M; Diamond TM; Kousseff BG
    Am J Med Genet; 1995 Nov; 59(3):271-5. PubMed ID: 8599348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
    Milunsky JM; Wyandt HE; Huang XL; Kang XZ; Elias ER; Milunsky A
    Am J Med Genet; 1996 Jan; 61(3):269-73. PubMed ID: 8741873
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
    Schlegel M; Baumer A; Riegel M; Wiedemann U; Schinzel A
    Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Advanced parental age in maternal uniparental disomy (UPD): implications for the mechanism of formation.
    Kotzot D
    Eur J Hum Genet; 2004 May; 12(5):343-6. PubMed ID: 14747835
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M; Tozzi C; Pomponi MG; Stagni ML; Della Monica M; Scarano G; Calvieri F; Torrisi L; Neri G
    Eur J Hum Genet; 1999; 7(4):421-6. PubMed ID: 10352932
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
    Menéndez I; Casaña H
    Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
    Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
    Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
    Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
    Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.
    Kotzot D
    Ann Genet; 2004; 47(3):251-60. PubMed ID: 15337470
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal UPD 20 in a hyperactive child with severe growth retardation.
    Chudoba I; Franke Y; Senger G; Sauerbrei G; Demuth S; Beensen V; Neumann A; Hansmann I; Claussen U
    Eur J Hum Genet; 1999 Jul; 7(5):533-40. PubMed ID: 10439958
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture.
    Harrison K; Eisenger K; Anyane-Yeboa K; Brown S
    Am J Med Genet; 1995 Aug; 58(2):147-51. PubMed ID: 8533806
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.
    Markovic VD; Chitayat DA; Ritchie SM; Chodakowski BA; Hutton EM
    Am J Med Genet; 1996 Feb; 61(4):363-70. PubMed ID: 8834049
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
    Grati FR; Grimi B; Frascoli G; Di Meco AM; Liuti R; Milani S; Trotta A; Dulcetti F; Grosso E; Miozzo M; Maggi F; Simoni G
    Eur J Hum Genet; 2006 Mar; 14(3):282-8. PubMed ID: 16418738
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
    Font-Montgomery E; Stone KM; Weaver DD; Vance GH; Das S; Thurston VC
    Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):577-82. PubMed ID: 16007591
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16.
    Schneider AS; Bischoff FZ; McCaskill C; Coady ML; Stopfer JE; Shaffer LG
    Am J Med Genet; 1996 Dec; 66(2):204-8. PubMed ID: 8958332
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.