BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 11415513)

  • 21. The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females.
    Kubota T; Wakui K; Nakamura T; Ohashi H; Watanabe Y; Yoshino M; Kida T; Okamoto N; Matsumura M; Muroya K; Ogata T; Goto Y; Fukushima Y
    Cytogenet Genome Res; 2002; 99(1-4):276-84. PubMed ID: 12900575
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Three patients with ring (X) chromosomes and a severe phenotype.
    Dennis NR; Collins AL; Crolla JA; Cockwell AE; Fisher AM; Jacobs PA
    J Med Genet; 1993 Jun; 30(6):482-6. PubMed ID: 8326492
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
    Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ
    J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.
    Migeon BR; Luo S; Jani M; Jeppesen P
    Am J Hum Genet; 1994 Sep; 55(3):497-504. PubMed ID: 8079992
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Turner syndrome and mosaicism].
    Battin J
    Bull Acad Natl Med; 2003; 187(2):359-67; discussion 368-70. PubMed ID: 14556446
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Assessment of X bends in patients with atypical X chromosome phenotypes.
    Munn CA; Wenger SL; Steele MW
    Ann Genet; 1991; 34(2):120-4. PubMed ID: 1746882
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
    Wolff DJ; Brown CJ; Schwartz S; Duncan AM; Surti U; Willard HF
    Am J Hum Genet; 1994 Jul; 55(1):87-95. PubMed ID: 8023855
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.
    Uematsu A; Yorifuji T; Muroi J; Kawai M; Mamada M; Kaji M; Yamanaka C; Momoi T; Nakahata T
    Am J Med Genet; 2002 Aug; 111(2):134-9. PubMed ID: 12210339
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.
    Gunther DF; Eugster E; Zagar AJ; Bryant CG; Davenport ML; Quigley CA
    Pediatrics; 2004 Sep; 114(3):640-4. PubMed ID: 15342833
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Supernumerary chromosomes in mosaic Turner syndrome.
    Thong MK; Manonmani V; Norlasiah IS
    Med J Malaysia; 1996 Dec; 51(4):487-90. PubMed ID: 10968041
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression.
    Stankiewicz P; Thiele H; Giannakudis I; Schlicker M; Baldermann C; Krüger A; Dörr S; Starke H; Hansmann I
    Am J Med Genet; 2001 Aug; 102(3):286-92. PubMed ID: 11484209
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotype and X inactivation in 45,X/46,X,r(X) cases.
    Leppig KA; Sybert VP; Ross JL; Cunniff C; Trejo T; Raskind WH; Disteche CM
    Am J Med Genet A; 2004 Jul; 128A(3):276-84. PubMed ID: 15216549
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mosaic ring Y chromosome in two normal healthy men with azoospermia.
    Bertini V; Canale D; Bicocchi MP; Simi P; Valetto A
    Fertil Steril; 2005 Dec; 84(6):1744. PubMed ID: 16359976
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.
    Stavropoulou C; Mignon C; Delobel B; Moncla A; Depetris D; Croquette MF; Mattei MG
    J Med Genet; 1998 Nov; 35(11):932-8. PubMed ID: 9832041
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evidence from skewed X inactivation for trisomy mosaicism in Silver-Russell syndrome.
    Sharp A; Moore G; Eggermann T
    Eur J Hum Genet; 2001 Dec; 9(12):887-91. PubMed ID: 11840189
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature.
    Bertini V; Valetto A; Uccelli A; Tarantino E; Simi P
    Fertil Steril; 2008 Nov; 90(5):2004.e1-5. PubMed ID: 18371955
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Epigenetic aspects of X-chromosome dosage compensation.
    Park Y; Kuroda MI
    Science; 2001 Aug; 293(5532):1083-5. PubMed ID: 11498577
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.