BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

249 related articles for article (PubMed ID: 27759572)

  • 21. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partial monosomy 1q43 and partial trisomy 20q13.2: a case report.
    Ho BS; McCready E; Nowaczyk MJ
    Clin Dysmorphol; 2016 Jul; 25(3):128-32. PubMed ID: 27057655
    [No Abstract]   [Full Text] [Related]  

  • 23. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [TBL] [Abstract][Full Text] [Related]  

  • 24. De novo trisomy 20p of paternal origin.
    Chaabouni M; Turleau C; Karboul L; Jemaa LB; Maazoul F; Attié-Bitach T; Romana S; Chaabouni H
    Am J Med Genet A; 2007 May; 143A(10):1100-3. PubMed ID: 17431912
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome.
    Watanabe S; Shimizu K; Ohashi H; Kosaki R; Okamoto N; Shimojima K; Yamamoto T; Chinen Y; Mizuno S; Dowa Y; Shiomi N; Toda Y; Tashiro K; Shichijo K; Minatozaki K; Aso S; Minagawa K; Hiraki Y; Shimokawa O; Matsumoto T; Fukuda M; Moriuchi H; Yoshiura K; Kondoh T
    Am J Med Genet A; 2016 Apr; 170A(4):908-17. PubMed ID: 26782913
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Identification of two de novo partial trisomies by comparative genomic hybridization.
    Rigola MA; Carrera M; Ribas I; De La Iglesia C; Mendez B; Egozcue J; Fuster C
    Clin Genet; 2001 Feb; 59(2):106-10. PubMed ID: 11260211
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings.
    Hagen A; Bigl A; Wand D; Klopocki E; Heller R; Siekmeyer M; Siekmeyer W; Kiess W; Merkenschlager A
    Am J Med Genet A; 2011 Dec; 155A(12):3075-81. PubMed ID: 22052712
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.
    Emberger W; Petek E; Kroisel PM; Zierler H; Wagner K
    Am J Med Genet; 2001 Dec; 104(4):312-8. PubMed ID: 11754067
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.
    Semerci CN; Cinbis M; Ullmann R; Steininger A; Bahce M; Yagci B; Ozden S; Sabir N; Gumus D; Tepeli E; Arteaga J; Mutchinick OM
    Am J Med Genet A; 2010 Jul; 152A(7):1724-9. PubMed ID: 20578131
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotypic overlapping of trisomy 12p and Pallister-Killian syndrome.
    Inage E; Suzuki M; Minowa K; Akimoto N; Hisata K; Shoji H; Okumura A; Shimojima K; Shimizu T; Yamamoto T
    Eur J Med Genet; 2010; 53(3):159-61. PubMed ID: 20219705
    [TBL] [Abstract][Full Text] [Related]  

  • 33. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
    Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
    Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A case of de novo partial tetrasomy of distal 6p and review of the literature.
    Stohler R; Kucharski E; Farrow E; Torres-Martinez W; Delk P; Thurston VC; Vance GH
    Am J Med Genet A; 2007 Sep; 143A(17):1978-83. PubMed ID: 17663466
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
    Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
    [TBL] [Abstract][Full Text] [Related]  

  • 36. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
    Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence.
    Valdes-Miranda JM; Soto-Alvarez JR; Toral-Lopez J; González-Huerta L; Perez-Cabrera A; Gonzalez-Monfil G; Messina-Bass O; Cuevas-Covarrubias S
    Eur J Med Genet; 2014 Feb; 57(2-3):60-4. PubMed ID: 24503149
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
    Akalin I; Bozdag S; Spielmann M; Basaran SY; Nanda I; Klopocki E
    Am J Med Genet A; 2014 Feb; 164A(2):490-4. PubMed ID: 24311106
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
    Wieczorek D; Bartsch O; Gillessen-Kaesbach G
    Am J Med Genet A; 2003 Jul; 120A(3):429-33. PubMed ID: 12838568
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy].
    Qin F; Lu X; Feng Y; Tang P; Niu G; Li F; Zhang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):231-4. PubMed ID: 27060323
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.