These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 20964129)

  • 1. Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q.
    Chen CP; Tsai FJ; Lee CC; Chen WL; Pan CW; Wu PC; Wang W
    Genet Couns; 2010; 21(3):353-7. PubMed ID: 20964129
    [No Abstract]   [Full Text] [Related]  

  • 2. Paracentric inversion of Yq and review of the literature.
    Aiello V; Astolfi N; Gruppioni R; Buldrini B; Prontera P; Bonfatti A; Sensi A; Calzolari E
    Genet Couns; 2007; 18(4):379-82. PubMed ID: 18286818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two extra euchromatic bands in the qh region of chromosome 9.
    Ozkinay F; Ercal D; Ozkinay C; Onay H; Bora E; Erler A
    Genet Couns; 2005; 16(1):45-8. PubMed ID: 15844778
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.
    Ilgin Ruhi H; Tükün A; Karabulut H; Bayazit P; Bökesoy I
    Clin Genet; 2001 May; 59(5):368-70. PubMed ID: 11359472
    [No Abstract]   [Full Text] [Related]  

  • 6. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H; Cora T; Erkul I
    Genet Couns; 1999; 10(2):163-70. PubMed ID: 10422010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
    Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
    Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
    Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
    Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal detection of pericentric inversion of chromosome 12.
    Kim HJ; Levy J; Reguero W; Iu B; Wallach RC
    Diagn Gynecol Obstet; 1980; 2(3):231-4. PubMed ID: 7439022
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
    Mrózek K; Heinonen K; Theil KS; Bloomfield CD
    Genes Chromosomes Cancer; 2002 Jun; 34(2):137-53. PubMed ID: 11979548
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21.
    Chen CP; Lin CC; Ko TM; Tsai FJ; Chern SR; Lee CC; Chen YT; Wu PC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):377-80. PubMed ID: 21056330
    [No Abstract]   [Full Text] [Related]  

  • 14. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW
    Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature.
    Arn PH; Younie L; Russo S; Zackowski JL; Mankinen C; Estabrooks L
    Am J Med Genet; 1995 Jul; 57(3):420-4. PubMed ID: 7677144
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.
    Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK
    Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of partial trisomy 21 associated with maternal balanced translocation 46xx der 21 t(21q;22q) with pericentric inversion of chromosome 9.
    Parmar RC; Sira P
    J Postgrad Med; 2003; 49(2):154-6. PubMed ID: 12867693
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The usefulness of NOR and RFA banding in prenatal diagnosis: a case report.
    Sciorra LJ; Rajendra B; Cummings E; Ekblom L; Lee M
    Am J Med Genet; 1981; 10(2):147-9. PubMed ID: 7315871
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.