BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

580 related articles for article (PubMed ID: 20017317)

  • 1. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].
    Wen J; Liang D; Liao X; Xue J; Tang G; Xia Y; Long Z; Dai H; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):659-63. PubMed ID: 19953489
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
    Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
    Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
    Liang Y; Luo XP
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Origin and morphological features of small supernumerary marker chromosomes in Turner syndrome].
    Liu N; Tong T; Chen Y; Chen Y; Cai C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):43-46. PubMed ID: 29419858
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A; Blanco B; del Castillo V; Carnevale A
    Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
    Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
    Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype].
    Bocian E; Stańczak H; Wiśniewski A; Mazurczak T; Stankiewicz P
    Pediatr Pol; 1996 Mar; 71(3):203-9. PubMed ID: 8966091
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
    Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
    Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular cytogenetic study of Turner's syndrome with the 45, X/46,X,r(?) karyotype].
    Shi Y; Shi H; Ma S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Jun; 16(3):218-21. PubMed ID: 7805169
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
    Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
    Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
    Liehr T; Utine GE; Trautmann U; Rauch A; Kuechler A; Pietrzak J; Bocian E; Kosyakova N; Mrasek K; Boduroglu K; Weise A; Aktas D
    Cytogenet Genome Res; 2007; 118(1):31-7. PubMed ID: 17901697
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
    Huang Y; Sun X; Li Q
    Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
    Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
    Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.