BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 15750022)

  • 21. Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
    Liehr T; Mrasek K; Weise A; Dufke A; Rodríguez L; Martínez Guardia N; Sanchís A; Vermeesch JR; Ramel C; Polityko A; Haas OA; Anderson J; Claussen U; von Eggeling F; Starke H
    Cytogenet Genome Res; 2006; 112(1-2):23-34. PubMed ID: 16276087
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
    Blancato JK; Eglinton G; George J; Benkendorf J; Pinckert T; Meck J
    J Reprod Med; 1995 Jul; 40(7):537-9. PubMed ID: 7473445
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
    Starke H; Schreyer I; Kähler C; Fiedler W; Beensen V; Heller A; Nietzel A; Claussen U; Liehr T
    Prenat Diagn; 1999 Dec; 19(12):1169-74. PubMed ID: 10590438
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
    Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
    Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
    Starke H; Nietzel A; Weise A; Heller A; Mrasek K; Belitz B; Kelbova C; Volleth M; Albrecht B; Mitulla B; Trappe R; Bartels I; Adolph S; Dufke A; Singer S; Stumm M; Wegner RD; Seidel J; Schmidt A; Kuechler A; Schreyer I; Claussen U; von Eggeling F; Liehr T
    Hum Genet; 2003 Dec; 114(1):51-67. PubMed ID: 13680362
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.
    Guediche N; Tosca L; Nouchy M; Lecerf L; Cornet D; Brisset S; Goossens M; Tachdjian G
    Eur J Med Genet; 2012 Dec; 55(12):737-42. PubMed ID: 23017438
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient.
    Gulten T; Gorukmez O; Gorukmez O; Karkucak M; Ture M; Yakut T
    West Indian Med J; 2012 Dec; 61(9):924-7. PubMed ID: 24020236
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.
    Vraneković J; Brajenović-Milić B; Modrusan-Mozetić Z; Babić I; Kapović M
    Cytogenet Genome Res; 2008; 121(3-4):298-301. PubMed ID: 18758176
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
    Manolakos E; Kefalas K; Neroutsou R; Lagou M; Kosyakova N; Ewers E; Ziegler M; Weise A; Tsoplou P; Rapti SM; Papoulidis I; Anastasakis E; Garas A; Sotiriou S; Eleftheriades M; Peitsidis P; Malathrakis D; Thomaidis L; Kitsos G; Orru S; Liehr T; Petersen MB; Kitsiou-Tzeli S
    Mol Med Rep; 2010; 3(6):1015-22. PubMed ID: 21472348
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
    Liehr T; Starke H; Senger G; Melotte C; Weise A; Vermeesch JR
    Am J Med Genet A; 2006 Jan; 140(1):46-51. PubMed ID: 16333826
    [TBL] [Abstract][Full Text] [Related]  

  • 34. First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.
    Starke H; Mitulla B; Nietzel A; Heller A; Beensen V; Grosswendt G; Claussen U; von Eggeling F; Liehr T
    Am J Med Genet A; 2003 Jan; 116A(1):26-30. PubMed ID: 12476447
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):856-860. PubMed ID: 28040133
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
    Font-Montgomery E; Stone KM; Weaver DD; Vance GH; Das S; Thurston VC
    Birth Defects Res A Clin Mol Teratol; 2005 Aug; 73(8):577-82. PubMed ID: 16007591
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
    Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
    [TBL] [Abstract][Full Text] [Related]  

  • 39. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.