BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 18758176)

  • 21. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
    Liehr T; Mrasek K; Starke H; Claussen U; Schreiber G
    Cytogenet Genome Res; 2005; 111(2):179-81. PubMed ID: 16103662
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.
    Velinov M; Gu H; Genovese M; Duncan C; Warburton P; Brooks SS; Jenkins EC
    Ann Genet; 2004; 47(2):199-205. PubMed ID: 15183754
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial small supernumerary marker chromosome (sSMC) (14)(:p11-q11:) [corrected] in a child with translocation Down syndrome.
    Vundinti BR; Korgaonkar S; Ghosh K
    Indian J Pediatr; 2009 Dec; 76(12):1265-7. PubMed ID: 20012787
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
    Sillén A; Wadelius C; Annerén G
    Am J Med Genet; 1998 Nov; 80(2):163-8. PubMed ID: 9805135
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
    Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
    Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A dup(17)(p11.2p11.2) detected by fluorescence in situ hybridization in a boy with Alport syndrome.
    Balarin MA; da Silva Lopes VL; Varella-Garcia M
    Am J Med Genet; 1999 Jan; 82(2):183-6. PubMed ID: 9934986
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new small supernumerary marker chromosome involving 14pter → q12 in a child with severe neurodevelopmental retardation: case report and literature review.
    Qi M; Zhao Y; Wang Y; Li T
    Gene; 2013 Dec; 531(2):457-61. PubMed ID: 24013083
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Duplication 7p de novo and literature review.
    Zerres K; Schwanitz G; Gellissen K; Schroers L; Sohler R
    Ann Genet; 1989; 32(4):225-9. PubMed ID: 2692511
    [TBL] [Abstract][Full Text] [Related]  

  • 31. SKY assessment of two karyotypes with 0-6 supernumerary marker/ring chromosomes and review of previously reported cases with two or more markers.
    Reddy KS; Wang S; Groh S; Gonatos J
    Am J Med Genet A; 2003 Apr; 118A(2):156-71. PubMed ID: 12655496
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
    Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
    Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
    López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C
    Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
    Fickelscher I; Starke H; Schulze E; Ernst G; Kosyakova N; Mkrtchyan H; MacDermont K; Sebire N; Liehr T
    Prenat Diagn; 2007 Aug; 27(8):783-5. PubMed ID: 17546703
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Identification of human small supernumerary marker chromosomes and discussion of its research value].
    Ou J; Wang W; Duan CY; Fu WY; Liu YL; Sun J; Zhong HL; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):91-4. PubMed ID: 23450489
    [TBL] [Abstract][Full Text] [Related]  

  • 36. First report of a small supernumerary der(8;14) marker chromosome.
    Guilherme RS; Dutra AR; Perez AB; Takeno SS; Oliveira MM; Kulikowski LD; Klein E; Hamid AB; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 139(4):284-8. PubMed ID: 23548553
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mosaic trisomy (8)(p22 --> pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences.
    de Pater JM; Kroes HY; Verschuren M; van Oppen AC; Albrechts JC; Engelen JJ
    Prenat Diagn; 2005 Feb; 25(2):151-5. PubMed ID: 15712342
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
    Tönnies H; Pietrzak J; Bocian E; MacDermont K; Kuechler A; Belitz B; Trautmann U; Schmidt A; Schulze B; Rodríguez L; Binkert F; Yardin C; Kosyakova N; Volleth M; Mkrtchyan H; Schreyer I; von Eggeling F; Weise A; Mrasek K; Liehr T
    J Histochem Cytochem; 2007 Jun; 55(6):651-60. PubMed ID: 17341473
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
    Santos M; Mrasek K; Rigola MA; Starke H; Liehr T; Fuster C
    Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.