BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 16506277)

  • 1. Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.
    Boehm D; Laccone F; Burfeind P; Herold S; Schubert C; Zoll B; Männer J; Pauer HU; Bartels I
    Prenat Diagn; 2006 Mar; 26(3):286-90. PubMed ID: 16506277
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Nuchal thickening in Jacobsen syndrome.
    McClelland SM; Smith AP; Smith NC; Gray ES; Diack JS; Dean JC
    Ultrasound Obstet Gynecol; 1998 Oct; 12(4):280-2. PubMed ID: 9819862
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.
    Chen CP; Wang LK; Wu PC; Chang TY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Feb; 56(1):102-105. PubMed ID: 28254208
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.
    Chen CP; Chern SR; Tzen CY; Lee MS; Pan CW; Chang TY; Wang W
    Prenat Diagn; 2001 Apr; 21(4):317-20. PubMed ID: 11288126
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion.
    Böhm D; Hoffmann K; Laccone F; Wilken B; Dechent P; Frahm J; Bartels I; Bohlander SK
    Am J Med Genet A; 2006 Feb; 140(4):378-82. PubMed ID: 16419136
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
    Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ultrasonographic findings of facial dysmorphism in Wolf-Hirschhorn syndrome.
    Sase M; Hasegawa K; Honda R; Sumie M; Nakata M; Sugino N; Furukawa S
    Am J Perinatol; 2005 Feb; 22(2):99-102. PubMed ID: 15731989
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.
    Courtens W; Tjalma W; Messiaen L; Vamos E; Martin JJ; Van Bogaert E; Keersmaekers G; Meulyzer P; Wauters J
    Am J Med Genet; 1998 May; 77(3):188-97. PubMed ID: 9605585
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome.
    Wenger SL; Grossfeld PD; Siu BL; Coad JE; Keller FG; Hummel M
    Am J Med Genet A; 2006 Apr; 140(7):704-8. PubMed ID: 16502431
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
    Chen CP; Su YN; Lin SP; Chern SR; Su JW; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):120-4. PubMed ID: 23548232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal diagnosis of 17q12 microdeletion syndrome in fetal renal abnormalities].
    Jiang YL; Qi QW; Zhou XY; Geng FF; Bai JJ; Hao N; Liu JT
    Zhonghua Fu Chan Ke Za Zhi; 2017 Oct; 52(10):662-668. PubMed ID: 29060963
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial t(11;13)(q21;q14) and the duplication 11q, 13q phenotype.
    Park JP; McDermet MK; Doody AM; Marin-Padilla JM; Moeschler JB; Wurster-Hill DH
    Am J Med Genet; 1993 Jan; 45(1):46-8. PubMed ID: 8418658
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.