BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 7717422)

  • 1. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
    Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
    Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic variability of the cat eye syndrome. Case report and review of the literature.
    Rosias PR; Sijstermans JM; Theunissen PM; Pulles-Heintzberger CF; De Die-Smulders CE; Engelen JJ; Van Der Meer SB
    Genet Couns; 2001; 12(3):273-82. PubMed ID: 11693792
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
    Reiss JA; Weleber RG; Brown MG; Bangs CD; Lovrien EW; Magenis RE
    Am J Med Genet; 1985 Jan; 20(1):165-71. PubMed ID: 3970068
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.
    Magenis RE; Sheehy RR; Brown MG; McDermid HE; White BN; Zonana J; Weleber R
    Am J Med Genet; 1988 Jan; 29(1):9-19. PubMed ID: 3344779
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
    Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
    Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.
    Lindsay EA; Shaffer LG; Carrozzo R; Greenberg F; Baldini A
    Am J Med Genet; 1995 Apr; 56(3):296-9. PubMed ID: 7778594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Complex cyanotic heart defect in a newborn infant with cat eye syndrome].
    Paul T; Reimer A; Wilken M; Miller K; Kallfelz HC
    Monatsschr Kinderheilkd; 1991 Apr; 139(4):228-30. PubMed ID: 2072964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
    Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
    Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
    Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC; James RS; Patch C; Temple IK
    Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.
    Hassed SJ; Hopcus-Niccum D; Zhang L; Li S; Mulvihill JJ
    Clin Genet; 2004 May; 65(5):400-4. PubMed ID: 15099348
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL; Duncan AM; Khalifa MM
    Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial duplication 19p.
    Stratton RF; DuPont BR; Olsen AS; Fertitta A; Hoyer M; Moore CM
    Am J Med Genet; 1995 Jul; 57(4):562-4. PubMed ID: 7573129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
    Van Hove JL; McConkie-Rosell A; Chen YT; Iafolla AK; Lanman JT; Hennessy MD; Kahler SG
    Am J Med Genet; 1992 Sep; 44(1):24-30. PubMed ID: 1519645
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cytogenetic characterization of cat eye syndrome marker chromosome.
    Wenger SL; Surti U; Nwokoro NA; Steele MW
    Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints.
    McTaggart KE; Budarf ML; Driscoll DA; Emanuel BS; Ferreira P; McDermid HE
    Cytogenet Cell Genet; 1998; 81(3-4):222-8. PubMed ID: 9730608
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.