BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 10694686)

  • 21. Development and targeted application of a rapid QF-PCR test for sex chromosome imbalance.
    Donaghue C; Roberts A; Mann K; Ogilvie CM
    Prenat Diagn; 2003 Mar; 23(3):201-10. PubMed ID: 12627420
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
    Liehr T
    Methods Mol Biol; 2008; 444():27-38. PubMed ID: 18425469
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. 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]  

  • 25. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E; Chen PX; Thangavelu M; Fiddler M
    Prenat Diagn; 2000 Mar; 20(3):215-20. PubMed ID: 10719324
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
    Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
    Nataf V; Senat MV; Albert M; Bidat L; de Mazancourt P; Roume J; Allard L; Le Tessier D; Ville Y; Selva J
    Prenat Diagn; 2002 Aug; 22(8):675-80. PubMed ID: 12210575
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [An investigation of small marker chromosome in eight Turner syndrome patients by fluorescence in situ hybridization and DNA analysis].
    Hu X; Zhu B; Hu B; Lin H; Shu D; Li C; Liu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):392-4. PubMed ID: 10581353
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.
    Chen CP; Lin CC; Su YN; Tsai FJ; Chern SR; Lee CC; Chen WL; Chen LF; Wu PC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):381-4. PubMed ID: 21056331
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis.
    Jardim A; Melo JB; Matoso E; Pires LM; Ramos L; Carreira IM
    Prenat Diagn; 2007 Apr; 27(4):380-1. PubMed ID: 17393554
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
    Crolla JA; Youings SA; Ennis S; Jacobs PA
    Eur J Hum Genet; 2005 Feb; 13(2):154-60. PubMed ID: 15508017
    [TBL] [Abstract][Full Text] [Related]  

  • 35. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Are all phenotypically-normal Turner syndrome fetuses mosaics?
    Amiel A; Kidron D; Kedar I; Gaber E; Reish O; Fejgin MD
    Prenat Diagn; 1996 Sep; 16(9):791-5. PubMed ID: 8905892
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case report.
    Lohmann L; Chelloug N; Rosales B; Guérin C; Lyonnet S; Jonveaux P; Simon-Bouy B
    Prenat Diagn; 2000 Feb; 20(2):156-8. PubMed ID: 10694690
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. The significance of accessory bisatellited marker chromosomes in amniotic fluid cell cultures.
    Djalali M
    Ann Genet; 1990; 33(3):141-5. PubMed ID: 2288457
    [TBL] [Abstract][Full Text] [Related]  

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