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 *

196 related articles for article (PubMed ID: 19291777)

  • 1. The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues.
    Papavassiliou P; York TP; Gursoy N; Hill G; Nicely LV; Sundaram U; McClain A; Aggen SH; Eaves L; Riley B; Jackson-Cook C
    Am J Med Genet A; 2009 Feb; 149A(4):573-83. PubMed ID: 19291777
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Down syndrome: a study of chromosomal mosaicism.
    Modi D; Berde P; Bhartiya D
    Reprod Biomed Online; 2003 Jun; 6(4):499-503. PubMed ID: 12831601
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy 21-associated increases in chromosomal instability are unmasked by comparing isogenic trisomic/disomic leukocytes from people with mosaic Down syndrome.
    Rafferty K; Archer KJ; Turner K; Brown R; Jackson-Cook C
    PLoS One; 2021; 16(7):e0254806. PubMed ID: 34283872
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 21 Down syndrome. Parental mosaicism.
    Uchida IA; Freeman VC
    Hum Genet; 1985; 70(3):246-8. PubMed ID: 3160645
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V; Golden WL; von Kap-Herr C; Wilson WG
    Am J Med Genet; 1996 Mar; 62(1):38-41. PubMed ID: 8779322
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
    Wallerstein R; Yu MT; Neu RL; Benn P; Lee Bowen C; Crandall B; Disteche C; Donahue R; Harrison B; Hershey D; Higgins RR; Jenkins LS; Jackson-Cook C; Keitges E; Khodr G; Lin CC; Luthardt FW; Meisner L; Mengden G; Patil SR; Rodriguez M; Sciorra LJ; Shaffer LG; Stetten G; Van Dyke DL; Wang H
    Prenat Diagn; 2000 Feb; 20(2):103-22. PubMed ID: 10694683
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA; Schwartz S; Black CJ; Jaswaney V
    Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaicism in three cases of 47, XY (or XX), +i(18)(p10) detected by interphase FISH of buccal mucosa.
    Pfeiffer RA; Schulze T
    Ann Genet; 1994; 37(4):210-4. PubMed ID: 7710258
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal mosaicism in Down's syndrome: a diagnostic challenge.
    Ladda RL; Maisels MJ; Dossett JH; Dobelle Y
    Dev Med Child Neurol; 1977 Oct; 19(5):668-72. PubMed ID: 144078
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic Down syndrome in a patient with low-level mosaicism detected by microarray.
    Leon E; Zou YS; Milunsky JM
    Am J Med Genet A; 2010 Dec; 152A(12):3154-6. PubMed ID: 21108401
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child.
    DeLozier-Blanchet CD; Roeder E; Denis-Arrue R; Blouin JL; Low J; Fisher J; Scharnhorst D; Curry CJ
    Am J Med Genet; 2000 Dec; 95(5):444-9. PubMed ID: 11146464
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Incidence of mosaic cell lines in vivo and malsegregation of chromosome 21 in lymphocytes in vitro of trisomy 21 patients: detection by fluorescence in situ hybridization on binucleated lymphocytes.
    Shi Q; Adler ID; Zhang J; Zhang X; Shan X; Martin R
    Hum Genet; 2000 Jan; 106(1):29-35. PubMed ID: 10982178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones.
    Miller K; Arslan-Kirchner A; Schulze B; Dudel-Neujahr A; Morlot M; Burck U; Gerresheim F
    Ann Genet; 1997; 40(3):181-4. PubMed ID: 9401109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 8 mosaicism syndrome. Two cases demonstrating variability in phenotype.
    Kurtyka ZE; Krzykwa B; Piatkowska E; Radwan M; Pietrzyk JJ
    Clin Pediatr (Phila); 1988 Nov; 27(11):557-64. PubMed ID: 3180630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.
    Pavlicek J; Soucek O; Vrtel R; Klaskova E; Hana V; Stara V; Adamova K; Fürst T; Hana V; Kapralova S; Prochazka M; Snajderova M; Tomaskova H; Tüdös Z; Vrbicka D; Vrtel P; Zapletalova J; Tauber Z; Lebl J
    Horm Res Paediatr; 2022; 95(5):465-475. PubMed ID: 35970147
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Atypical Down syndrome phenotype with severe developmental delay, hypertonia, and seizures in a child with translocation trisomy 21.
    Keppler-Noreuil KM; Welch JL; Major HJ; Qiau Q; Jordan DK; Patil SR
    Dev Med Child Neurol; 2002 Jan; 44(1):64-7. PubMed ID: 11811653
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.
    Minelli A; Morerio C; Maserati E; Olivieri C; Panarello C; Bonvini L; Leszl A; Rosanda C; Lanino E; Danesino C; Pasquali F
    Leukemia; 2001 Jun; 15(6):971-5. PubMed ID: 11417485
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring.
    Frias S; Ramos S; Molina B; del Castillo V; Mayén DG
    Mutat Res; 2002 Sep; 520(1-2):25-37. PubMed ID: 12297141
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of a female with a peripheral blood lymphocytic karyotype of trisomy 18 but normal intelligence].
    Gao J; Yu X; Rong L; Mei B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):483-485. PubMed ID: 32219843
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.
    Chen CP; Wu FT; Pan YT; Wu PS; Chen WL; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2023 Nov; 62(6):891-895. PubMed ID: 38008510
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.