BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 15791680)

  • 1. Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
    Chen CP; Chang TY; Tzen CY; Wang W; Lee CC
    Prenat Diagn; 2005 Mar; 25(3):263-4. PubMed ID: 15791680
    [No Abstract]   [Full Text] [Related]  

  • 2. NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
    Chen CP; Chen YJ; Tsai FJ; Chern SR; Wang W
    Prenat Diagn; 2008 Apr; 28(4):364-5. PubMed ID: 18383001
    [No Abstract]   [Full Text] [Related]  

  • 3. Distal 10q trisomy associated with bilateral hydronephrosis in infancy.
    Chen CP; Lin SP
    Genet Couns; 2003; 14(3):359-62. PubMed ID: 14577683
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Lee CC; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):539-43. PubMed ID: 21199766
    [No Abstract]   [Full Text] [Related]  

  • 5. Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).
    Chen CP; Chern SR; Chang TY; Lee CC; Chen WL; Wang W
    Prenat Diagn; 2005 Nov; 25(11):1069-71. PubMed ID: 16302165
    [No Abstract]   [Full Text] [Related]  

  • 6. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
    Bregant L; Gersak K; Veble A
    Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
    Chen CP; Chen YJ; Chern SR; Tsai FJ; Chang TY; Lee CC; Town DD; Lee MS; Wang W
    Prenat Diagn; 2008 May; 28(5):450-3. PubMed ID: 18395879
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Prenatal diagnosis of sub-microscopic partial trisomy 10q using chromosomal microarray analysis in a phenotypically abnormal fetus with normal karyotype.
    Browne PC; Adam S; Badr M; Brooks CR; Edwards J; Walker P; Mohamed S; Gregg AR
    J Neonatal Perinatal Med; 2016 May; 9(2):217-22. PubMed ID: 27197934
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter).
    Batukan C; Ozgun MT; Basbug M; Caglayan O; Dundar M; Murat N
    Prenat Diagn; 2007 Apr; 27(4):365-8. PubMed ID: 17295347
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocation.
    Prabhakara K; Dutta U; Ramadevi AR
    Indian Pediatr; 2002 Nov; 39(11):1050-4. PubMed ID: 12466578
    [No Abstract]   [Full Text] [Related]  

  • 14. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy 10q with mild phenotype caused by an unbalanced X;10 translocation.
    Mononen T; Sharp A; Laakso M; Meltoranta RL; Valve-Dietz AK; Heinonen K
    J Med Genet; 2003 May; 40(5):e61. PubMed ID: 12746415
    [No Abstract]   [Full Text] [Related]  

  • 16. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O; Tastemir D
    Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distal trisomy 10q due to maternal insertional translocation (15;10): A case report and review of literature.
    Türedi Ö; Vícdan A; Yürür Kutlay N
    Genet Couns; 2016; 27(2):273-8. PubMed ID: 29485837
    [No Abstract]   [Full Text] [Related]  

  • 18. Unbalanced chromosomal translocation: a cause of recurrent spontaneous abortion.
    Zarina AL; Jamil MA; Ng SP; Rohana J; Yong SC; Salwati S; Boo NY
    Med J Malaysia; 2006 Jun; 61(2):260-2. PubMed ID: 16898328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 10p and translocation of 10q to 4p associated with selective dysgenesis of IgA-producing cells in lymphoid tissue.
    Saiga T; Hashimoto K; Kimura N; Ono H; Hiai H
    Pathol Int; 2007 Jan; 57(1):37-42. PubMed ID: 17199741
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)].
    Le Chevalier C; Chabrolle JP; Rossier A
    Ann Pediatr (Paris); 1978 Nov; 25(9):501-4, 507. PubMed ID: 16114368
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.