BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 9508064)

  • 21. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
    Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
    Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. 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]  

  • 25. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
    Nowaczyk MJ; Ramsay JA; Mohide P; Tomkins DJ
    Am J Med Genet; 1998 May; 77(4):306-9. PubMed ID: 9600741
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
    Vermeesch JR; Melotte C; Salden I; Riegel M; Trifnov V; Polityko A; Rumyantseva N; Naumchik I; Starke H; Matthijs G; Schinzel A; Fryns JP; Liehr T
    Eur J Med Genet; 2005; 48(3):319-27. PubMed ID: 16179227
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mosaic supernumerary r(8) syndrome.
    Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
    [No Abstract]   [Full Text] [Related]  

  • 28. Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.
    Matsuo M; Muroya K; Nanao K; Hasegawa Y; Terasaki H; Kosaki K; Ogata T
    Am J Med Genet; 2000 Apr; 91(4):267-72. PubMed ID: 10766981
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
    Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG; Pober BR; Gibson LH; Willis CR; McGrath J; Roberts DJ; Yang-Feng TL
    Am J Med Genet; 1995 Jan; 55(2):155-60. PubMed ID: 7717414
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Börjeson-Forssman-Lehmann syndrome in a woman with skewed X-chromosome inactivation.
    Kubota T; Oga S; Ohashi H; Iwamoto Y; Fukushima Y
    Am J Med Genet; 1999 Nov; 87(3):258-61. PubMed ID: 10564881
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 37. FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.
    Giardino D; Bettio D; Gottardi G; Rizzi N; Pierluigi M; Perfumo C; Calì A; Dagna Bricarelli F; Larizza L
    Am J Med Genet; 1999 Jun; 84(4):377-80. PubMed ID: 10340656
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
    Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
    Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
    [TBL] [Abstract][Full Text] [Related]  

  • 39. X chromosome inactivation and X-linked mental retardation.
    Willard HF
    Am J Med Genet; 1996 Jul; 64(1):21-6. PubMed ID: 8826443
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel ring chromosome composed of X- and Y-derived material in a girl with manifestations of Ullrich-Turner syndrome.
    Grass FS; Brown CA; Backeljauw PF; Lucas A; Brasington C; Gazak JM; Nakano S; Ostrowski RS; Spence JE
    Am J Med Genet; 2000 Aug; 93(5):343-8. PubMed ID: 10951455
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.