BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1546 related articles for article (PubMed ID: 16900777)

  • 21. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
    Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
    Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.
    Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S
    Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
    Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
    Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].
    Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M
    Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432
    [TBL] [Abstract][Full Text] [Related]  

  • 28. De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.
    Yakut S; Cetin Z; Berker-Karauzum S; Mihci E; Mendilcioglu I; Luleci G
    Genet Couns; 2011; 22(1):63-8. PubMed ID: 21614990
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
    Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.
    Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
    Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Cytogenic characterization of chromosome markers detected at amniocentesis: implications for karyotype-phenotype correlations].
    Valerio D; Aiello R; Altieri V; Antonucci F
    Minerva Ginecol; 1996 Sep; 48(9):365-9. PubMed ID: 8999384
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of mosaic tetrasomy 18p.
    Chen CP; Ko TM; Su YN; Chern SR; Su JW; Chen YT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Dec; 51(4):625-9. PubMed ID: 23276569
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
    Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
    Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
    Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
    Graf MD; Gill P; Krew M; Schwartz S
    Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
    Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 78.