BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 12813772)

  • 1. Prenatal diagnosis of de novo partial trisomy Xq (Xq22.1-->qter) and terminal Xp deletion following sonographic detection of intrauterine growth restriction.
    Chen CP
    Prenat Diagn; 2003 Jun; 23(6):518-9. PubMed ID: 12813772
    [No 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 and postnatal characterization of a de novo Xq22.1 terminal deletion.
    Vaglio A; Greif G; Bernal M; Sanguinetti C; Mechoso B; Quadrelli A; Tucci P; Milunsky JM; Huang XL; Pagano S; Quadrelli R
    Genet Test; 2006; 10(4):272-6. PubMed ID: 17253933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Lee MS; Wang W
    Prenat Diagn; 2003 May; 23(5):375-9. PubMed ID: 12749033
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
    Chen CP; Chern SR; Hsu CY; Lee CC; Lee MS; Wang W
    Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.
    Genesio R; De Brasi D; Conti A; Borghese A; Di Micco P; Di Costanzo P; Paladini D; Ungaro P; Nitsch L
    Am J Med Genet A; 2004 Aug; 128A(4):422-8. PubMed ID: 15264291
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
    Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosis.
    Tharapel AT; Moretti ML; Meyers CM; Shulman LP; Tipton RE; Summitt JB; Elias S; Wilroy RS; Epps M; Simpson JL
    Am J Perinatol; 1990 Jul; 7(3):211-3. PubMed ID: 2372326
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Lee CC; Chen YJ; Wang W
    Prenat Diagn; 2005 Aug; 25(8):723-5. PubMed ID: 16049995
    [No Abstract]   [Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.
    Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Wang W
    Gene; 2013 Mar; 516(1):138-42. PubMed ID: 23266815
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
    Boog G; Le Vaillant C; Collet M; Dupré PF; Parent P; Bongain A; Benoit B; Trastour C
    Fetal Diagn Ther; 2004; 19(5):421-30. PubMed ID: 15305099
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
    Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
    Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
    Chen CP; Chern SR; Chang TY; Lee CC; Chen LF; Tzen CY; Wang W; Lin CJ; Yang BP; Yang LS
    Prenat Diagn; 2003 Jan; 23(1):40-3. PubMed ID: 12533811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Recombinant X chromosome in a prenatal diagnosis.
    Orellana C; Badía L; Martínez F; Oltra JS; Monfort S; Roselló M; Cervera JV; García Z; Prieto F
    Cytogenet Genome Res; 2006; 112(3-4):337-40. PubMed ID: 16484792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.