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 *

135 related articles for article (PubMed ID: 10076888)

  • 1. Maternal uniparental disomy of chromosome 21 in a normal child.
    Rogan PK; Sabol DW; Punnett HH
    Am J Med Genet; 1999 Mar; 83(1):69-71. PubMed ID: 10076888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation.
    Miyoshi O; Hayashi S; Fujimoto M; Tomita H; Sohda M; Niikawa N
    J Hum Genet; 1998; 43(2):138-42. PubMed ID: 9621521
    [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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosis.
    Soler A; Margarit E; Queralt R; Carrió A; Costa D; Gómez D; Ballesta F
    Am J Med Genet; 2000 Feb; 90(4):291-3. PubMed ID: 10710225
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Paternal uniparental disomy for chromosome 14: a case report and review.
    Cotter PD; Kaffe S; McCurdy LD; Jhaveri M; Willner JP; Hirschhorn K
    Am J Med Genet; 1997 May; 70(1):74-9. PubMed ID: 9129745
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early embryonic failure associated with uniparental disomy for human chromosome 21.
    Henderson DJ; Sherman LS; Loughna SC; Bennett PR; Moore GE
    Hum Mol Genet; 1994 Aug; 3(8):1373-6. PubMed ID: 7987317
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up.
    Sanlaville D; Aubry MC; Dumez Y; Nolen MC; Amiel J; Pinson MP; Lyonnet S; Munnich A; Vekemans M; Morichon-Delvallez N
    J Med Genet; 2000 Jul; 37(7):525-8. PubMed ID: 10882756
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Normal phenotype with paternal uniparental isodisomy for chromosome 21.
    Blouin JL; Avramopoulos D; Pangalos C; Antonarakis SE
    Am J Hum Genet; 1993 Nov; 53(5):1074-8. PubMed ID: 8213833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure.
    Mulchandani S; Bhoj EJ; Luo M; Powell-Hamilton N; Jenny K; Gripp KW; Elbracht M; Eggermann T; Turner CL; Temple IK; Mackay DJ; Dubbs H; Stevenson DA; Slattery L; Zackai EH; Spinner NB; Krantz ID; Conlin LK
    Genet Med; 2016 Apr; 18(4):309-15. PubMed ID: 26248010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Uniparental disomy (UPD). Genomic imprinting and a case for new genetics (prenatal and clinical implications: the "Likon" concept).
    Engel E
    Ann Genet; 1997; 40(1):24-34. PubMed ID: 9150847
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.
    Nicholls RD; Pai GS; Gottlieb W; Cantú ES
    Ann Neurol; 1992 Oct; 32(4):512-8. PubMed ID: 1360787
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.
    Sachwitz J; Strobl-Wildemann G; Fekete G; Ambrozaitytė L; Kučinskas V; Soellner L; Begemann M; Eggermann T
    BMC Med Genet; 2016 Mar; 17():20. PubMed ID: 26969265
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.
    Langlois S; Yong SL; Wilson RD; Kwong LC; Kalousek DK
    J Med Genet; 1995 Nov; 32(11):871-5. PubMed ID: 8592330
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.