BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 18226135)

  • 1. De novo 7q deletion with a positive maternal serum triple test screening.
    Park IY; Jo YS; Shin JC; Sung IK; Kim M
    J Obstet Gynaecol Res; 2008 Feb; 34(1):85-7. PubMed ID: 18226135
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intermediate interstitial deletion of chromosome 7q detected by first-trimester Down's syndrome screening.
    Cheong ML; Tsai MS; Cortes RA; Harrison MR
    Fetal Diagn Ther; 2008; 24(4):340-4. PubMed ID: 18841024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Chen LF; Wang W
    Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
    Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
    Chen CP; Chern SR; Liu FF; Jan SW; Lee CC; Chang YC; Yue CT
    Prenat Diagn; 1997 Jun; 17(6):571-6. PubMed ID: 9203216
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.
    Le Caignec C; Winer N; Boceno M; Delnatte C; Podevin G; Liet JM; Quere MP; Joubert M; Rival JM
    Prenat Diagn; 2003 Dec; 23(12):981-4. PubMed ID: 14663834
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Serum screening of fetal chromosome abnormality during second pregnancy trimester: results of 26,803 pregnant women in Jiangsu Province].
    Hu YL;
    Zhonghua Yi Xue Za Zhi; 2007 Sep; 87(35):2476-80. PubMed ID: 18067809
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Experience on triple markers serum screening for Down's syndrome fetus in Hat Yai, Regional Hospital.
    Lamlertkittikul S; Chandeying V
    J Med Assoc Thai; 2007 Oct; 90(10):1970-6. PubMed ID: 18041410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus.
    Bijlsma EK; Knegt AC; Bilardo CM; Goodman FR
    Prenat Diagn; 2005 Jan; 25(1):39-44. PubMed ID: 15662696
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Prenatal diagnosis of 47,XXX.
    Khoury-Collado F; Wehbeh AN; Fisher AJ; Bombard AT; Weiner Z
    Am J Obstet Gynecol; 2005 May; 192(5):1469-71. PubMed ID: 15902140
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P; Jüttnerová V; Jarosová M; Fialová J; Fiedler Z; Kolmanová J
    Cas Lek Cesk; 2001 Mar; 140(4):122-4. PubMed ID: 11284430
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
    Chen CP; Chern SR; Lee CC; Chen LF; Chin DT; Tzen CY; Wang W
    Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of a partial monosomy 7q11-->q31 in a fetus with split foot.
    Yilmaz Z; Eroğlu D; Derbent M; Haberal AN; Lembet A; Sahin FI
    Fetal Diagn Ther; 2005; 20(2):132-5. PubMed ID: 15692208
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.
    Yakut S; Cetin Z; Simşek M; Karaüzüm SB; Tükün A; Lüleci G
    Genet Couns; 2009; 20(4):327-32. PubMed ID: 20162867
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.