BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 3239584)

  • 1. Partial trisomy 9--further delineation of the phenotype.
    Smart RD; Viljoen DL; Fraser B
    Am J Med Genet; 1988 Dec; 31(4):947-51. PubMed ID: 3239584
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN; Raj A; Baker D
    Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy 22: no longer an enigma.
    Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
    Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32.
    Kleczkowska A; Fryns JP; Lemay P; Van den Berghe H
    Genet Couns; 1993; 4(3):217-21. PubMed ID: 8267931
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G; Decock P; Fryns JP
    Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].
    de Grouchy J; Turleau C; Danis F; Kohout G; Briard ML
    Ann Genet; 1978 Dec; 21(4):247-51. PubMed ID: 314266
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
    Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B; Moore R; Mohandas T
    Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24.
    Halpern GJ; Shohat M; Merlob P
    Ann Genet; 1996; 39(3):181-3. PubMed ID: 8839892
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A new case of trisomy 5p].
    Antonenko VG; Levina LIa; Chudnova VI
    Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
    Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of partial trisomy 9 (9pter-->q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly.
    Chen CP; Hsu CH; Lin SP; Ho CS; Lee CC; Wang W
    Prenat Diagn; 2003 Jun; 23(6):519-20. PubMed ID: 12813773
    [No Abstract]   [Full Text] [Related]  

  • 15. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Phenotype of trisomy 9].
    Pfeiffer RA; Müller R
    Monatsschr Kinderheilkd; 1984 Oct; 132(10):797-800. PubMed ID: 6513939
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.
    Jelin A; Perry H; Hogue J; Oberoi S; Cotter PD; Klein OD
    J Craniofac Surg; 2010 Sep; 21(5):1376-9. PubMed ID: 20856024
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C; Meck JM
    Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 9 mosaicism syndrome. A case report and review of the literature.
    Tarani L; Colloridi F; Raguso G; Rizzuti A; Bruni L; Tozzi MC; Palermo D; Panero A; Vignetti P
    Ann Genet; 1994; 37(1):14-20. PubMed ID: 8010707
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial proximal trisomy 10q syndrome: a new case.
    Nucaro A; Faedda A; Cao A; Boccone L
    Genet Couns; 2002; 13(4):411-6. PubMed ID: 12558111
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.