BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

85 related articles for article (PubMed ID: 27751441)

  • 1. Distal trisomy 3q as a risk factor for neural tube defects.
    Lurie I
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):769-770. PubMed ID: 27751441
    [No Abstract]   [Full Text] [Related]  

  • 2. Neural tube defects and omphalocele in trisomy 18.
    van Maldergem L; Gillerot Y; Koulischer L
    Clin Genet; 1989 Jan; 35(1):77-8. PubMed ID: 2924433
    [No Abstract]   [Full Text] [Related]  

  • 3. Recurrent neural tube defects associated with partial trisomy 2p22-pter: report of two siblings and review of the literature.
    Doray B; Favre R; Gasser B; Girard-Lemaire F; Schluth C; Flori E
    Genet Couns; 2003; 14(2):165-72. PubMed ID: 12872810
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neural tube defects, chromosome abnormalities and multiple closure sites for the human neural tube.
    Seller MJ
    Clin Dysmorphol; 1995 Jul; 4(3):202-7. PubMed ID: 7551155
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
    Chen CP; Chen YJ; Chern SR; Tsai FJ; Lin HH; Lee CC; Wang W
    Prenat Diagn; 2008 Sep; 28(9):865-7. PubMed ID: 18661486
    [No Abstract]   [Full Text] [Related]  

  • 6. Neural tube defects in chromosomally normal and abnormal human embryos.
    Coerdt W; Miller K; Holzgreve W; Rauskolb R; Schwinger E; Rehder H
    Ultrasound Obstet Gynecol; 1997 Dec; 10(6):410-5. PubMed ID: 9476327
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 18 and neural tube defects.
    Rosa RF; Trevisan P; Rosa RC; Lorenzen MB; Zen PR; Oliveira CA; Graziadio C; Paskulin GA
    Pediatr Neurol; 2013 Sep; 49(3):203-4. PubMed ID: 23831245
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy 13 syndrome and neural tube defects.
    Rodríguez JI; García M; Morales C; Morillo A; Delicado A
    Am J Med Genet; 1990 Aug; 36(4):513-6. PubMed ID: 2202219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q.
    Chen CP; Lee CC; Chuang CY; Town DD; Lee MS; Chen MH
    Clin Genet; 1997 Sep; 52(3):196-8. PubMed ID: 9377814
    [No Abstract]   [Full Text] [Related]  

  • 10. Concomitant partial tetrasomy 3q and trisomy 18 in Waldenström macroglobulinemia.
    Wong KF; Kwong YL; Wong TK
    Cancer Genet Cytogenet; 1995 May; 81(1):92-3. PubMed ID: 7773966
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Karyotyping for isolated neural tube defects. A report of two cases.
    O'Reilly GC; Shields LE
    J Reprod Med; 2000 Nov; 45(11):950-2. PubMed ID: 11127112
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy 3 is a specific genomic aberration of t(14;18) negative follicular lymphoma.
    Tagawa H; Karube K; Guo Y; Takeshita M; Kikuchi M; Morishima Y; Nakamura S; Ohshima K; Seto M
    Leukemia; 2007 Dec; 21(12):2549-51. PubMed ID: 17611568
    [No Abstract]   [Full Text] [Related]  

  • 14. Neural tube defects in trisomy 18.
    Nisani R; Chemke J; Cohen-Ankori H; Nissim F
    Prenat Diagn; 1981 Jul; 1(3):227-31. PubMed ID: 7346824
    [No Abstract]   [Full Text] [Related]  

  • 15. Trisomy 18 and 13 screening: consequences for the Dutch Down syndrome screening programme.
    Koster MP; Stoutenbeek P; Visser GH; Schielen PC
    Prenat Diagn; 2010 Mar; 30(3):287-9. PubMed ID: 20112231
    [No Abstract]   [Full Text] [Related]  

  • 16. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
    Sepulveda W; Corral E; Ayala C; Be C; Gutierrez J; Vasquez P
    Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Maternal serum screening in Ontario using the triple marker test.
    Summers AM; Farrell SA; Huang T; Meier C; Wyatt PR
    J Med Screen; 2003; 10(3):107-11. PubMed ID: 14561260
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents.
    Tonni G; Azzoni D; Panteghini M; Ventura A; Cavalli P
    Congenit Anom (Kyoto); 2007 Sep; 47(3):101-4. PubMed ID: 17688469
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma.
    Torlakovic EE; Aamot HV; Heim S
    J Pathol; 2006 Jun; 209(2):258-64. PubMed ID: 16583359
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.