BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 12210328)

  • 1. Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
    Angle B; Yen F; Hersh JH; Gowans G; Barch M
    Am J Med Genet; 2002 Aug; 111(3):307-12. PubMed ID: 12210328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM; Sekhon GS; Laxova R
    Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypes.
    Celle L; Lee L; Rintoul N; Savani RC; Long W; Mennuti MT; Krantz ID
    Am J Med Genet; 2000 Sep; 94(2):125-40. PubMed ID: 10982969
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Monozygotic twins discordant for partial trisomy 1.
    Watson WJ; Katz VL; Albright SG; Rao KW; Aylsworth AS
    Obstet Gynecol; 1990 Nov; 76(5 Pt 2):949-51. PubMed ID: 2216262
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
    Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
    Vincent MC; Heitz F; Tricoire J; Bourrouillou G; Kuhlein E; Rolland M; Calvas P
    Genet Couns; 1999; 10(1):43-9. PubMed ID: 10191428
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
    Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
    [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. Partial duplication of 4q12q13 leads to a mild phenotype.
    Shashi V; Berry MN; Santos C; Pettenati MJ
    Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further contribution to the description of phenotypes associated with partial 4q duplication.
    Zollino M; Zampino G; Torrioli G; Pomponi MG; Neri G
    Am J Med Genet; 1995 May; 57(1):69-73. PubMed ID: 7645603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.
    Isidor B; Le Cunff M; Boceno M; Boisseau P; Thomas C; Rival JM; David A; Le Caignec C
    Eur J Med Genet; 2008; 51(6):679-84. PubMed ID: 18672103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication.
    Parentin F; Fabretto A; Benussi DG; Petix V; Marchetti F; Dalprà L; Redaelli S; Pensiero S; Pecile V
    Ophthalmic Genet; 2009 Jun; 30(2):103-5. PubMed ID: 19373683
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
    Estop AM; Bansal V; Lin A; Levinson F; Karlin SM; Surti U; Wenger SL; Steele MW
    Am J Med Genet; 1994 Feb; 49(4):410-3. PubMed ID: 8160735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay.
    Rashidi-Nezhad A; Parvaneh N; Farzanfar F; Azimi C; Harewood L; Akrami SM; Reymond A
    Eur J Med Genet; 2012 Mar; 55(3):203-10. PubMed ID: 22370062
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.
    Lu JH; Chung MY; Hwang B; Chien HP
    Pediatr Cardiol; 2001; 22(3):260-3. PubMed ID: 11343161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies.
    Wakita Y; Narahara K; Tsuji K; Yokoyama Y; Ninomiya S; Murakami R; Kikkawa K; Seino Y
    Hum Genet; 1992 Mar; 88(5):596-8. PubMed ID: 1551663
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication of (12)(pter-q13.3) combined with deletion of (22)(pter-q11.2) in a patient with features of both chromosome aberrations.
    Tyshchenko NA; Riegel M; Evseenkova EG; Zerova TE; Gorovenko NG; Schinzel A
    Eur J Med Genet; 2007; 50(2):128-32. PubMed ID: 17174617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report.
    Sandal G; Ormeci AR; Oztas S
    Genet Couns; 2013; 24(2):217-22. PubMed ID: 24032293
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.