BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 11288126)

  • 1. 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]  

  • 2. Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.
    Chen CP; Wang TH; Lin CC; Tsai FJ; Hsieh LJ; Wang W
    J Formos Med Assoc; 2008 Oct; 107(10):822-6. PubMed ID: 18926951
    [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 interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones.
    Chen CP; Chern SR; Lee CC; Chen LF; Chuang CY
    Prenat Diagn; 1998 May; 18(5):490-5. PubMed ID: 9621384
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound.
    Chen CP; Hsu CY; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):763-765. PubMed ID: 32917333
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.
    Chen CP; Chang TY; Hung FY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):843-846. PubMed ID: 29241932
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].
    Doray B; Badila-Timbolschi D; Schaefer E; Fattori D; Monga B; Dott B; Favre R; Kohler M; Nisand I; Viville B; Kauffmann I; Bruant-Rodier C; Grollemund B; Rinkenbach R; Astruc D; Gasser B; Lindner V; Marcellin L; Flori E; Girard-Lemaire F; Dollfus H
    Arch Pediatr; 2012 Oct; 19(10):1021-9. PubMed ID: 22925539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene.
    Sun M; Lou J; Li Q; Chen J; Li Y; Li D; Yuan H; Liu Y
    Taiwan J Obstet Gynecol; 2019 Mar; 58(2):292-295. PubMed ID: 30910156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses.
    Bergé SJ; Plath H; Van de Vondel PT; Appel T; Niederhagen B; Von Lindern JJ; Reich RH; Hansmann M
    Ultrasound Obstet Gynecol; 2001 Nov; 18(5):422-31. PubMed ID: 11844159
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Mild pyelectasis ascertained with prenatal ultrasonography is pediatrically significant.
    Persutte WH; Koyle M; Lenke RR; Klas J; Ryan C; Hobbins JC
    Ultrasound Obstet Gynecol; 1997 Jul; 10(1):12-8. PubMed ID: 9263417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Ultrasonographic features of orofacial clefts at first trimester of pregnancy: report of two cases].
    Picone O; de Keersmaecker B; Ville Y
    J Gynecol Obstet Biol Reprod (Paris); 2003 Dec; 32(8 Pt 1):736-9. PubMed ID: 15067898
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Problems posed by the diagnosis and prenatal management of facial clefts].
    Perrotin F; Lardy H; Marret H; Paillet C; Lansac J; Body G
    Rev Stomatol Chir Maxillofac; 2001 Jun; 102(3-4):143-52. PubMed ID: 11577466
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.