BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 7516121)

  • 1. Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
    Schrander-Stumpel CT; Govaerts LC; Engelen JJ; van der Blij-Philipsen M; Borghgraef M; Loots WJ; Peters JJ; Rijnvos WP; Smeets DF; Fryns JP
    Am J Med Genet; 1994 May; 50(4):377-80. PubMed ID: 7516121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mosaic tetrasomy 8p.
    Newton D; Hammond L; Wiley J; Kushnick T
    Am J Med Genet; 1993 Jun; 46(5):513-6. PubMed ID: 8322811
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 32(3):320-4. PubMed ID: 2729351
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
    Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
    Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels.
    Fisher AM; Barber JC; Crolla JA; James RS; Lestas AN; Jennings I; Dennis NR
    Am J Med Genet; 1993 Aug; 47(1):100-5. PubMed ID: 8368238
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].
    Sijmons RH; Leegte B; van Lingen RA; de Pater JM; van der Veen AY; del Canho H; Bos C; ten Kate LP; Breed AS
    Am J Med Genet; 1993 Sep; 47(4):559-62. PubMed ID: 7504882
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Concurrence of inv(7)(q11.2q32) and del(8)(p23.1) in a girl with congenital microcephaly, hypotonia, developmental delay, strabismus, hypernatremia, hypermagnesemia and deafness.
    Mahjoubi F; Nasiri F; Razazian F
    Genet Couns; 2012; 23(3):397-404. PubMed ID: 23072189
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
    Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic isochromosome 8p.
    Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
    Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.
    Kleczkowska A; Fryns JP; D'Hondt F; Jaeken J; Van den Berghe H
    Ann Genet; 1987; 30(1):47-51. PubMed ID: 3498429
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
    Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
    Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD; Hansen KL; Littlefield CA
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 68(4):481-4. PubMed ID: 9021026
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 63(3):482-5. PubMed ID: 8737657
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
    Reddy KS; Sulcova V; Schwartz S; Noble JE; Phillips J; Brasel JA; Huff K; Lin HJ
    Am J Med Genet; 2000 May; 92(1):69-76. PubMed ID: 10797426
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mosaic "tetrasomy" 8p: case report and review of the literature.
    Winters J; Markello T; Nance W; Jackson-Cook C
    Clin Genet; 1995 Oct; 48(4):195-8. PubMed ID: 8591671
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.
    Choo S; Teo SH; Tan M; Yong MH; Ho LY
    J Perinatol; 2002; 22(5):420-3. PubMed ID: 12082482
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.
    Merritt TA; Natarajan G
    Am J Perinatol; 2007 Oct; 24(9):563-6. PubMed ID: 17893842
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.