BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

350 related articles for article (PubMed ID: 12575013)

  • 1. Tetrasomy 12p--unusual presentation in CVS.
    Dong L; Falk RE; Williams J; Kohan M; Schreck RR
    Prenat Diagn; 2003 Feb; 23(2):101-3. PubMed ID: 12575013
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
    Polityko AD; Goncharova E; Shamgina L; Drozdovskaja N; Podleschuk L; Abramchik E; Jaroshevich E; Khurs O; Pisarik I; Pribushenya O; Rumyantseva N; Naumchik I
    J Histochem Cytochem; 2005 Mar; 53(3):361-4. PubMed ID: 15750020
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS.
    Bernert J; Bartels I; Gatz G; Hansmann I; Heyat M; Niedmann PD; Rehder H; Waldenmaier C; Zoll B
    Am J Med Genet; 1992 Mar; 42(5):747-50. PubMed ID: 1632452
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
    Gerdes AM; Hansen LK; Brandrup F; Soegaard K; Christoffersen A; Rasmussen K
    Pediatr Dermatol; 2006; 23(4):378-81. PubMed ID: 16918638
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
    de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
    Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Post-zygotic origin of isochromosome 12p.
    de Ravel TJ; Keymolen K; van Assche E; Wittevronghel I; Moerman P; Salden I; Matthijs G; Fryns JP; Vermeesch JR
    Prenat Diagn; 2004 Dec; 24(12):984-8. PubMed ID: 15614858
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
    Horn D; Majewski F; Hildebrandt B; Körner H
    J Med Genet; 1995 Jan; 32(1):68-71. PubMed ID: 7897632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
    Wegner RD; Schröck E; Obladen M; Becker R; Stumm M; Sperling K
    Prenat Diagn; 1996 Aug; 16(8):741-8. PubMed ID: 8878285
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
    Wilson SC; Susman M; Bain S; Wohlferd M; Van Dyke D; Daniel A; White B; Gardner RJ
    Prenat Diagn; 2002 Aug; 22(8):681-5. PubMed ID: 12210576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.
    Libotte F; Bizzoco D; Gabrielli I; Mesoraca A; Cignini P; Vitale SG; Marilli I; Gulino FA; Rapisarda AM; Giorlandino C
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.
    Ward BE; Hayden MW; Robinson A
    Am J Med Genet; 1988 Dec; 31(4):835-9. PubMed ID: 3239575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
    Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
    Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
    Wu YC; Fang JS; Lee KF; Estipona J; Yang ML; Yuan CC
    Prenat Diagn; 2003 Feb; 23(2):124-7. PubMed ID: 12575018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation.
    Frković SH; Durisević IT; Trcić RL; Sarnavka V; Gornik KC; Muzinić D; Letica L; Barić I; Begović D
    Coll Antropol; 2010 Mar; 34(1):247-50. PubMed ID: 20437642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
    Slater HR; Vaux C; Pertile M; Burgess T; Petrovic V
    Prenat Diagn; 1997 Feb; 17(2):109-13. PubMed ID: 9061757
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.