BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 15198723)

  • 1. No sex differences in 18 trisomy births in the Kanagawa Birth Defects Monitoring Program.
    Kuroki Y; Kurosawa K
    Congenit Anom (Kyoto); 2004 Jun; 44(2):97-8. PubMed ID: 15198723
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [20 cases of trisomy 18. Sex-ratio in relation to age of the mother].
    Le Marec BM; Lair JC; Kérisit J; Le Mée F; Sénécal J
    Ann Pediatr (Paris); 1977 Feb; 24(2):125-36. PubMed ID: 16211953
    [No Abstract]   [Full Text] [Related]  

  • 3. Associated malformations in cases with neural tube defects.
    Stoll C; Alembik Y; Dott B
    Genet Couns; 2007; 18(2):209-15. PubMed ID: 17710873
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Potential impact of pregnancy outcome on the completeness of diagnosis of birth defects, Hawai'i, 1986-2001.
    Forrester MB; Merz RD
    Hawaii Med J; 2007 Feb; 66(2):32, 34-5. PubMed ID: 17393915
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
    Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 18 with multiple rare malformations: report of one case.
    Su PH; Chen JY; Hsu CH; Chen SJ; Chan SW; Lin LL
    Acta Paediatr Taiwan; 2007; 48(5):272-5. PubMed ID: 18254577
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Positive biochemical screening for trisomy 18: on the path of trisomy 9.
    Póvoa A; Ramalho C; Torgal A; Brandão O; Matias A; Oliveira MJ; Montenegro N; Castedo S
    Prenat Diagn; 2008 Feb; 28(2):162-4. PubMed ID: 18236431
    [No Abstract]   [Full Text] [Related]  

  • 8. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
    Langlois S; Yong PJ; Yong SL; Barrett I; Kalousek DK; Miny P; Exeler R; Morris K; Robinson WP
    Prenat Diagn; 2006 Jun; 26(6):548-58. PubMed ID: 16683298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Follow up and evaluation of the Victorian first-trimester combined screening programme for Down syndrome and trisomy 18.
    Jaques AM; Halliday JL; Francis I; Bonacquisto L; Forbes R; Cronin A; Sheffield LJ
    BJOG; 2007 Jul; 114(7):812-8. PubMed ID: 17501960
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [When infants are born dead: "It has come and has left behind its marks"].
    Lucassen H
    Pflege Z; 2004 Jan; 57(1):10-3. PubMed ID: 14768160
    [No Abstract]   [Full Text] [Related]  

  • 11. Edwards syndrome with double trisomy.
    Tennakoon J; Kandasamy Y; Alcock G; Koh TH
    Singapore Med J; 2008 Jul; 49(7):e190-1. PubMed ID: 18695855
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Trisomy 18 associated with atrioventricular canal].
    Digilio MC; Marino B; Giannotti A; Dallapiccola B
    G Ital Cardiol; 1991 Apr; 21(4):433-5. PubMed ID: 1936748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
    Neiswanger K; Hohler PM; Hively-Thomas LB; McPherson EW; Hogge WA; Surti U
    Prenat Diagn; 2006 May; 26(5):454-61. PubMed ID: 16557642
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
    Bornstein E; Barnhard Y; Donnenfeld A; Ferber A; Divon MY
    Obstet Gynecol; 2006 Apr; 107(4):877-9. PubMed ID: 16582126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18.
    Taysi K; Hatiboğlu N; Halicioglu C; Say B
    Turk J Pediatr; 1972 Oct; 14(4):141-5. PubMed ID: 16295083
    [No Abstract]   [Full Text] [Related]  

  • 16. Using record linkage and manual follow-up to evaluate the Victorian maternal serum screening quadruple test for Down's syndrome, trisomy 18 and neural tube defects.
    Jaques AM; Collins VR; Haynes K; Sheffield LJ; Francis I; Forbes R; Halliday JL
    J Med Screen; 2006; 13(1):8-13. PubMed ID: 16569299
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
    Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cardiovascular malformations among preterm infants.
    Tanner K; Sabrine N; Wren C
    Pediatrics; 2005 Dec; 116(6):e833-8. PubMed ID: 16322141
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening for trisomy 18 by maternal age, fetal nuchal translucency, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A.
    Kagan KO; Wright D; Maiz N; Pandeva I; Nicolaides KH
    Ultrasound Obstet Gynecol; 2008 Sep; 32(4):488-92. PubMed ID: 18726925
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18].
    Stoll C; Messer J
    Ann Pediatr (Paris); 1979 Jan; 26(1):38-40. PubMed ID: 16106870
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.