BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 11536263)

  • 21. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
    Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
    Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
    Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
    Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
    Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A; Fourneau C; Dugauquier C; Rombout S; Sartenaer D; Gillerot Y
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of trisomy 1q21-qter: case report and review of literature.
    Machlitt A; Kuepferling P; Bommer C; Koerner H; Chaoui R
    Am J Med Genet A; 2005 Apr; 134A(2):207-11. PubMed ID: 15704122
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings.
    Cakmak-Genc G; Karakas-Celik S; Dursun A; Piskin İE
    Gene; 2015 Sep; 568(2):211-4. PubMed ID: 25979671
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 1q44-qter trisomy: clinical report and review of the literature.
    Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9).
    Hengstschläger M; Bettelheim D; Repa C; Lang S; Deutinger J; Bernaschek G
    Fetal Diagn Ther; 2002; 17(4):243-6. PubMed ID: 12065954
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
    Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
    Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations.
    Speleman F; Callens B; Logghe K; Van Roy N; Horsley SW; Jauch A; Verschraegen-Spae MR; Leroy JG
    Am J Med Genet; 2000 Aug; 93(5):349-54. PubMed ID: 10951456
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis of der(11)t(11;18)(q24;q21.3) due to paternal balanced translocation and both parents are carriers of alpha-thalassemia-1--a case report.
    Chao MC; Yang SY; Chang Y; Huang YW; Liu TC; Lee JP; Chen BH
    Kaohsiung J Med Sci; 2001 Aug; 17(8):430-6. PubMed ID: 11715843
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Duplication/deletion mosaicism of the 7q(21.1 --> 31.3) region.
    Morales C; Madrigal I; Esqué T; de la Fuente JE; Rodríguez JM; Margarit E; Soler A; Sánchez A
    Am J Med Genet A; 2007 Jan; 143A(2):179-83. PubMed ID: 17163539
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation.
    Atik T; Durmaz B; Yorganci OU; Cogulu O; Kioutsouk M; Ozkinay F
    Genet Couns; 2013; 24(2):179-84. PubMed ID: 24032288
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
    Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.