BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 1363214)

  • 1. Mosaic ring chromosome 13 analyzed by fluorescence in situ hybridization: report of a case.
    Hou JW; Liu CH; Wang TR; Zhu HM; Jiang S; Sciorra LJ; Lee ML
    J Formos Med Assoc; 1992 Nov; 91(11):1108-11. PubMed ID: 1363214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
    Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
    Su PH; Chen CP; Su YN; Chen SJ; Lin LL; Chen JY
    Genet Mol Res; 2013 Apr; 12(2):1311-7. PubMed ID: 23661454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ring chromosome 22 and autism: report and review.
    MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
    Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial ring (19) chromosome mosaicism: case report and review.
    Flejter WL; Finlinson D; Root S; Nguyen W; Brothman AR; Viskochil D
    Am J Med Genet; 1996 Dec; 66(3):276-80. PubMed ID: 8985487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X).
    Manea SR; Gershin IF; Babu A; Willner JP; Desnick RJ; Cotter PD
    Clin Genet; 1997 Dec; 52(6):432-5. PubMed ID: 9520254
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.
    Levy B; Jalal SM; Dunn TM; Warburton PE; Tonk VS; Hirschhorn K; Lockhart LH; Hughes T; Velagaleti GV
    Am J Med Genet; 2002 Mar; 108(3):198-204. PubMed ID: 11891685
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).
    Blennow E; Annerén G; Bui TH; Berggren E; Asadi E; Nordenskjöld M
    Am J Hum Genet; 1993 Aug; 53(2):433-42. PubMed ID: 8328459
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis.
    Hou JW
    Chang Gung Med J; 2004 May; 27(5):373-8. PubMed ID: 15366814
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L; Jackson J; Cowell C; Sillence D; Smith A
    Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature.
    Sivasankaran A; Kanakavalli MK; Anuradha D; Samuel CR; Kandukuri LR
    Cytogenet Genome Res; 2016; 148(2-3):165-73. PubMed ID: 27222354
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
    Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
    Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
    Nowaczyk MJ; Ramsay JA; Mohide P; Tomkins DJ
    Am J Med Genet; 1998 May; 77(4):306-9. PubMed ID: 9600741
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inherited ring chromosome 8 without loss of subtelomeric sequences.
    Le Caignec C; Boceno M; Jacquemont S; Nguyen The Tich S; Rival JM; David A
    Ann Genet; 2004; 47(3):289-96. PubMed ID: 15337475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
    Louvrier C; Egea G; Labalme A; Des Portes V; Gazzo S; Callet-Bauchu E; Till M; Sanlaville D; Edery P; Schluth-Bolard C
    Cytogenet Genome Res; 2015; 147(2-3):111-7. PubMed ID: 26669311
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
    Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.