BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

94 related articles for article (PubMed ID: 19375526)

  • 41. Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
    Güven GS; Fenerci EY; Deviren A; Ozkiliç A; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2004; 15(3):321-8. PubMed ID: 15517825
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
    Chen CP; Lin SP; Tsai FJ; Wang TH; Chern SR; Wang W
    Fertil Steril; 2008 Oct; 90(4):1198.e11-8. PubMed ID: 18304539
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Persistent gestational trophoblastic disease after an androgenetic/biparental fetal chimera: a case report and review.
    Surti U; Hoffner L; Kolthoff M; Dunn J; Hunt J; Sniezek L; Macpherson T
    Int J Gynecol Pathol; 2006 Oct; 25(4):366-72. PubMed ID: 16990714
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
    Lunghi M; Casorzo L; De Paoli L; Riccomagno P; Rossi D; Gaidano G
    Cancer Genet Cytogenet; 2010 Jan; 196(1):89-92. PubMed ID: 19963141
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Dysgerminoma in a pure 45,X Turner syndrome: report of a case and review of the literature.
    Pierga JY; Giacchetti S; Vilain E; Extra JM; Brice P; Espie M; Maragi JA; Fellous M; Marty M
    Gynecol Oncol; 1994 Dec; 55(3 Pt 1):459-64. PubMed ID: 7835789
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
    Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
    Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Y-specific sequences in Turner syndrome].
    Slezak R; Sasiadek M; Dobosz T; Gogulska L; Jagielski J
    Ginekol Pol; 1999 Sep; 70(9):610-6. PubMed ID: 10534924
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.
    Bruyère H; Speevak MD; Winsor EJ; de Fréminville B; Farrell SA; McGowan-Jordan J; McGillivray B; Chitayat D; McFadden D; Adouard V; Terespolsky D; Prieur F; Pantzar T; Hrynchak M
    Prenat Diagn; 2006 Apr; 26(4):324-9. PubMed ID: 16521154
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
    Höckner M; Pinggera GM; Günther B; Sergi C; Fauth C; Erdel M; Kotzot D
    Fertil Steril; 2008 Nov; 90(5):2009.e13-7. PubMed ID: 18687426
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases.
    Struthers JL; Cuthbert CD; Khalifa MM
    Am J Med Genet; 1999 May; 84(2):111-5. PubMed ID: 10323734
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Ring chromosome X in a child with manifestations of Kabuki syndrome.
    McGinniss MJ; Brown DH; Burke LW; Mascarello JT; Jones MC
    Am J Med Genet; 1997 May; 70(1):37-42. PubMed ID: 9129739
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Y chromosome in Turner syndrome].
    Rojek A; Kwasiuk K; Obara-Moszyńska M; Kolesińska Z; Niedziela M
    Pediatr Endocrinol Diabetes Metab; 2017; 23(1):37-41. PubMed ID: 29073306
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Constitutional telomeric association (Y;7) in a patient with a female phenotype.
    Beneteau C; Baron S; David A; Jossic F; Poulain D; Schmitt S; Leclair MD; Piloquet P; Le Caignec C
    Am J Med Genet A; 2013 Jun; 161A(6):1436-41. PubMed ID: 23613342
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Deletion (2)(q37).
    Stratton RF; Tolworthy JA; Young RS
    Am J Med Genet; 1994 Jun; 51(2):153-5. PubMed ID: 8092193
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Genetic considerations in the patient with Turner syndrome--45,X with or without mosaicism.
    Zhong Q; Layman LC
    Fertil Steril; 2012 Oct; 98(4):775-9. PubMed ID: 23020909
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.
    Reddy KS; Yang X
    Am J Med Genet A; 2003 Mar; 117A(3):261-7. PubMed ID: 12599190
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature.
    Tang R; Lin L; Guo Z; Hou H; Yu Q
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00732. PubMed ID: 31070017
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Dicentric Y chromosomes. First part: cytogenetic and molecular aspects].
    Bouayed Abdelmoula N; Amouri A
    Ann Biol Clin (Paris); 2005; 63(3):263-78. PubMed ID: 15951258
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Nongonadal neoplasia in patients with Turner syndrome.
    Sivakumaran TA; Ghose S; Kumar H; Singha U; Kucheria K
    J Environ Pathol Toxicol Oncol; 1999; 18(4):339-47. PubMed ID: 15281247
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.