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 *

167 related articles for article (PubMed ID: 10740212)

  • 1. Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation.
    Petek E; Wagner K; Steiner H; Schaffer H; Kroisel PM
    Prenat Diagn; 2000 Apr; 20(4):349-52. PubMed ID: 10740212
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Chern SR; Chen WM; Lee CC; Hsieh LJ; Wang W
    Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
    Chen CP; Chen YJ; Chern SR; Tsai FJ; Chang TY; Lee CC; Town DD; Lee MS; Wang W
    Prenat Diagn; 2008 May; 28(5):450-3. PubMed ID: 18395879
    [No Abstract]   [Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
    Lee C; Fowler DJ; Lemyre E; Sandstrom MM; Holmes LB; Morton CC
    Am J Med Genet; 2001 May; 100(3):246-50. PubMed ID: 11343311
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
    Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
    Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.
    Cambosu F; Capobianco G; Fogu G; Bandiera P; Pirino A; Moro MA; Sanna R; Soro G; Dessole M; Montella A
    J Obstet Gynaecol Res; 2013 Feb; 39(2):592-7. PubMed ID: 22925348
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes.
    Tapper JK; Zhang S; Harirah HM; Panova NI; Merryman LS; Hawkins JC; Lockhart LH; Gei AB; Velagaleti GV
    Fetal Diagn Ther; 2002; 17(6):347-51. PubMed ID: 12393964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis.
    Chen CP; Lee CC; Pan CW; Kir TY; Chen BF
    Prenat Diagn; 1998 Dec; 18(12):1289-93. PubMed ID: 9885021
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qter.
    Tchirikov M; Merinsky A; Strohner M; Bonin M; Beyer V; Haaf T; Bartsch O
    Am J Med Genet A; 2010 Mar; 152A(3):721-5. PubMed ID: 20186810
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
    Zafra de la Rosa G; Venegas-Vega CA; Monroy N; Contreras-Bucio G; Friedrich U; Houman M; Saad A; Fernández P; Kofman-Alfaro S; Cervantes A
    Am J Med Genet A; 2005 Jul; 136(3):259-64. PubMed ID: 15957183
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
    Chen CP; Lin CC; Chang TY; Li YC; Hsieh LJ; Lee CC; Chen LF; Wang W
    Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
    [No Abstract]   [Full Text] [Related]  

  • 16. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
    Dundar M; Uzak A; Saatci C; Akalin H
    Genet Couns; 2011; 22(3):287-92. PubMed ID: 22029170
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
    Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
    Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.