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Journal Abstract Search
265 related items for PubMed ID: 8882781
1. Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant. Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM. Am J Med Genet; 1996 Mar 29; 62(3):243-6. PubMed ID: 8882781 [Abstract] [Full Text] [Related]
2. Homozygous alpha-thalassemia with trisomy 7 mosaicism in a live-born infant. Quintero-Rivera F, Abreu-E-Lima P, Zhang IH, Parast MM. Pediatr Hematol Oncol; 2009 Sep 29; 26(6):426-31. PubMed ID: 19657992 [Abstract] [Full Text] [Related]
3. "Mosaic trachea" in a child with trisomy 9 mosaicism. Gniady JP, Isaacson G, Ladda RL. Int J Pediatr Otorhinolaryngol; 2010 Oct 29; 74(10):1193-5. PubMed ID: 20727599 [Abstract] [Full Text] [Related]
4. 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 01; 62(1):38-41. PubMed ID: 8779322 [Abstract] [Full Text] [Related]
5. Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature. Cantú ES, Eicher DJ, Pai GS, Donahue CJ, Harley RA. Am J Med Genet; 1996 Apr 24; 62(4):330-5. PubMed ID: 8723059 [Abstract] [Full Text] [Related]
6. Trisomy 9 mosaicism in a girl with multiple malformations. Diaz-Mares L, Molina B, Carnevale A. Ann Genet; 1990 Apr 24; 33(3):165-8. PubMed ID: 2288462 [Abstract] [Full Text] [Related]
7. Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girl. Lorda-Sánchez I, Villa A, Urioste M, Bernal E, Jaso E, García A, Martínez-Frías ML. Am J Med Genet; 1997 Feb 11; 68(4):481-4. PubMed ID: 9021026 [Abstract] [Full Text] [Related]
8. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype. Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G. Prenat Diagn; 2003 Feb 11; 23(2):128-33. PubMed ID: 12575019 [Abstract] [Full Text] [Related]
9. Secondary trisomy or mosaic "tetrasomy" 8p. Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW. Am J Med Genet; 1989 Mar 11; 32(3):320-4. PubMed ID: 2729351 [Abstract] [Full Text] [Related]
10. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies. Van den Enden A, Verschraegen-Spae MR, Van Roy N, Decaluwe W, De Praeter C, Speleman F. Am J Med Genet; 1996 Jun 14; 63(3):482-5. PubMed ID: 8737657 [Abstract] [Full Text] [Related]
11. 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 22; 61(3):269-73. PubMed ID: 8741873 [Abstract] [Full Text] [Related]
12. Tetraploidy: a report of three live-born infants. Scarbrough PR, Hersh J, Kukolich MK, Carroll AJ, Finley SC, Hochberger R, Wilkerson S, Yen FF, Althaus BW. Am J Med Genet; 1984 Sep 22; 19(1):29-37. PubMed ID: 6496571 [Abstract] [Full Text] [Related]
13. 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 Sep 22; 7(4):421-6. PubMed ID: 10352932 [Abstract] [Full Text] [Related]
14. Variable clinical expression of mosaic trisomy 16 in the newborn infant. Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P. Am J Med Genet; 1993 Aug 15; 47(2):294-8. PubMed ID: 8213923 [Abstract] [Full Text] [Related]
15. MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype. Wilson GN, Vekemans MJ, Kaplan P. Am J Med Genet; 1988 Aug 15; 30(4):953-61. PubMed ID: 3055989 [Abstract] [Full Text] [Related]
16. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case. Martínez A, Ramos S, González-del Angel A, Alcántara MA, Molina B, Carnevale A. Rev Invest Clin; 2007 Aug 15; 59(6):444-8. PubMed ID: 18402336 [Abstract] [Full Text] [Related]
17. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis. Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H. Pediatr Dermatol; 2004 Aug 15; 21(6):636-41. PubMed ID: 15575846 [Abstract] [Full Text] [Related]
18. Delineation of a clinical syndrome caused by mosaic trisomy 15. Bühler EM, Bienz G, Straumann E, Bösch N. Am J Med Genet; 1996 Mar 15; 62(2):109-12. PubMed ID: 8882390 [Abstract] [Full Text] [Related]
19. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. Leichtman LG, Zackowski JL, Storto PD, Newlin A. Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648 [Abstract] [Full Text] [Related]
20. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations. Wilson WG, Shires MA, Willson KA, Wyandt HE, Harris LM, Kelly TE. Am J Med Genet; 1983 Sep 14; 16(1):131-6. PubMed ID: 6638063 [Abstract] [Full Text] [Related] Page: [Next] [New Search]