BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 10073907)

  • 1. Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.
    Faivre L; Morichon-Delvallez N; Viot G; Martinovic J; Pinson MP; Aubry JP; Raclin V; Edery P; Dumez Y; Munnich A; Vekemans M
    Prenat Diagn; 1999 Jan; 19(1):49-53. PubMed ID: 10073907
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.
    Malan V; Martinovic J; Sanlaville D; Caillat S; Waill MC; Ganne ML; Tantau J; Attie-Bitach T; Vekemans M; Morichon-Delvallez N
    Prenat Diagn; 2006 Mar; 26(3):231-8. PubMed ID: 16450350
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
    Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
    Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M; Martinovic J; Sanlaville D; Attié-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
    Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review.
    Prontera P; Clerici G; Bernardini L; Schippa M; Capalbo A; Manes I; Giuffrida MG; Barbieri MG; Ardisia C; Donti E
    Genet Couns; 2011; 22(1):41-8. PubMed ID: 21614987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal detection of cyclopia associated with interstitial deletion of 2p.
    Grundy HO; Niemeyer P; Rupani MK; Ward VF; Wassman ER
    Am J Med Genet; 1989 Oct; 34(2):268-70. PubMed ID: 2817010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prenatal diagnosis of deletion of chromosome 6p presenting with hydrops fetalis.
    Suwanrath-Kengpol C; Limprasert P; Mitarnun W
    Prenat Diagn; 2004 Nov; 24(11):887-9. PubMed ID: 15565585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
    Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of mosaicism for 11q terminal deletion.
    Valduga M; Cannard VL; Philippe C; Romana S; Miton A; Droulle P; Foliguet B; Lecompte T; Jonveaux P
    Eur J Med Genet; 2007; 50(6):475-81. PubMed ID: 17761465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal detection of deletion 6q13q15 in a complex karyotype.
    Yu M; Obringer AC; Fowler MH; Hummel M; Wenger SL
    Prenat Diagn; 2005 Dec; 25(12):1084-7. PubMed ID: 16231325
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
    Peng HH; Wang TH; Hsueh DW; Chang SD; Soong YK
    Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of a 4q33-4qter deletion in a fetus with hydrops.
    Russell Z; Kontopoulos EV; Quintero RA; DeBauche DM; Ranells JD
    Fetal Diagn Ther; 2008; 24(3):250-3. PubMed ID: 18765938
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and characterization of an analphoid marker chromosome 16.
    Tabet AC; Gosset P; Elghezal H; Fontaine S; Martinovic J; Encha Razavi F; Romana S; Vekemans M; Morichon-Delvallez N
    Prenat Diagn; 2004 Sep; 24(9):733-6. PubMed ID: 15386469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature.
    Faivre L; Morichon-Delvallez N; Viot G; Narcy F; Loison S; Mandelbrot L; Aubry MC; Raclin V; Edery P; Munnich A; Vekemans M
    Prenat Diagn; 1998 Oct; 18(10):1055-60. PubMed ID: 9826897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
    Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.