BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

402 related articles for article (PubMed ID: 15503276)

  • 1. A rare case of de novo distal 19q trisomy prenatally diagnosed.
    Rombout S; Sartenaer D; Parmentier B; Dugauquier C; Gillerot Y
    Prenat Diagn; 2004 Oct; 24(10):822-7. PubMed ID: 15503276
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatally diagnosed trisomy 6 mosaicism.
    Gupta N; Pradhan M; Manisha ; Singh R; Phadke SR
    Prenat Diagn; 2004 Oct; 24(10):841-4. PubMed ID: 15503282
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 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. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 6. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
    Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P; Korniszewski L; Bocian E; Stańczak H
    Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP; Porter HJ; Young ID
    Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
    Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM; Tan YQ; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of complete trisomy 19q.
    Babić I; Brajenović-Milić B; Petrović O; Mustać E; Kapović M
    Prenat Diagn; 2007 Jul; 27(7):644-7. PubMed ID: 17437325
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of trisomy 3 mosaicism.
    Zaslav AL; Pierno G; Davis J; Fougner A; Jacob J; Kazi R; Blumenthal D; Sturim S; Shaham M; Fox J
    Prenat Diagn; 2004 Sep; 24(9):693-6. PubMed ID: 15386452
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
    Mercier S; Fellmann F; Cattin J; Bresson JL
    Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
    Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.