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 *

254 related articles for article (PubMed ID: 8541876)

  • 1. Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis.
    Ledbetter DH; Engel E
    Hum Mol Genet; 1995; 4 Spec No():1757-64. PubMed ID: 8541876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies.
    Yong PJ; Marion SA; Barrett IJ; Kalousek DK; Robinson WP
    Am J Med Genet; 2002 Oct; 112(2):123-32. PubMed ID: 12244544
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and genetic counseling of uniparental disomy.
    Chien SC; Chen CP; Liou JD
    Taiwan J Obstet Gynecol; 2022 Mar; 61(2):210-215. PubMed ID: 35361378
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.
    Berend SA; Feldman GL; McCaskill C; Czarnecki P; Van Dyke DL; Shaffer LG
    Am J Med Genet; 1999 Jan; 82(3):275-81. PubMed ID: 10215554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Uniparental disomy of multiple chromosomes in two cases with a complex phenotype.
    Polonis K; Lopes JL; Cabral H; Babcock HE; Kline L; Ruiz KM; Schwartz S; Hasadsri L; Rowsey RA; Hoppman NL; Grant CL
    Am J Med Genet A; 2023 Jul; 191(7):1978-1983. PubMed ID: 37134191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself.
    Scheuvens R; Begemann M; Soellner L; Meschede D; Raabe-Meyer G; Elbracht M; Schubert R; Eggermann T
    Clin Genet; 2017 Jul; 92(1):45-51. PubMed ID: 28032339
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing.
    Yip MY
    Transl Pediatr; 2014 Apr; 3(2):98-107. PubMed ID: 26835328
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.
    Silverstein S; Lerer I; Sagi M; Frumkin A; Ben-Neriah Z; Abeliovich D
    Prenat Diagn; 2002 Aug; 22(8):649-51. PubMed ID: 12210570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Uniparental disomy and Robertsonian translocations: risk estimation and prenatal testing.
    Eggermann T; Zerres K
    Mol Diagn; 2003; 7(2):113-7. PubMed ID: 14580230
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.
    Kotzot D
    Am J Med Genet; 1999 Jan; 82(3):265-74. PubMed ID: 10215553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Robertsonian translocations: mechanisms of formation, aneuploidy, and uniparental disomy and diagnostic considerations.
    Kim SR; Shaffer LG
    Genet Test; 2002; 6(3):163-8. PubMed ID: 12490055
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
    Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH
    Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Risk estimates for uniparental disomy following prenatal detection of a nonhomologous Robertsonian translocation.
    Shaffer LG
    Prenat Diagn; 2006 Apr; 26(4):303-7. PubMed ID: 16491515
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternal uniparental isodisomy for chromosome 14 detected prenatally.
    Ralph A; Scott F; Tiernan C; Caubere M; Kollegger S; Junio J; Roberts C; Ewen K; Slater HR
    Prenat Diagn; 1999 Jul; 19(7):681-4. PubMed ID: 10419621
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cytogenetic and age-dependent risk factors associated with uniparental disomy 15.
    Robinson WP; Langlois S; Schuffenhauer S; Horsthemke B; Michaelis RC; Christian S; Ledbetter DH; Schinzel A
    Prenat Diagn; 1996 Sep; 16(9):837-44. PubMed ID: 8905898
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
    Ruggeri A; Dulcetti F; Miozzo M; Grati FR; Grimi B; Bellato S; Natacci F; Maggi F; Simoni G
    Prenat Diagn; 2004 Dec; 24(12):997-1000. PubMed ID: 15614836
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes.
    Berend SA; Horwitz J; McCaskill C; Shaffer LG
    Am J Hum Genet; 2000 Jun; 66(6):1787-93. PubMed ID: 10775524
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.