BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 21542309)

  • 21. [Chromosome aberrations in abortions].
    Boué JG; Boué A; Lazar P
    Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690
    [No Abstract]   [Full Text] [Related]  

  • 22. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.
    Robinson WP; Bernasconi F; Lau A; McFadden DE
    Am J Med Genet; 1999 May; 84(1):34-42. PubMed ID: 10213044
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Trisomy 16 and trisomy 16 Mosaicism: a review.
    Benn P
    Am J Med Genet; 1998 Sep; 79(2):121-33. PubMed ID: 9741470
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Spontaneous abortion: cytogenetic study of 609 cases].
    Be C; Velásquez P; Youlton R
    Rev Med Chil; 1997 Mar; 125(3):317-22. PubMed ID: 9460269
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Studies on phenotype, development, and viability of human spontaneous abortuses with acrocentric trisomies and polyploidies: with reference to the relationship of the viability to the origin of extrachromosomes (author's transl)].
    Niikawa N
    Hokkaido Igaku Zasshi; 1979 May; 54(3):235-44. PubMed ID: 521006
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.
    Peñaherrera MS; Barrett IJ; Brown CJ; Langlois S; Yong SL; Lewis S; Bruyère H; Howard-Peebles PN; Kalousek DK; Robinson WP
    Clin Genet; 2000 Dec; 58(6):436-46. PubMed ID: 11149612
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Lethal chromosome abnormalities in the antenatal and perinatal stages of human development].
    Petrov-Maslakov MA; Golovachev GD
    Vestn Akad Med Nauk SSSR; 1972; 27(5):68-77. PubMed ID: 5074593
    [No Abstract]   [Full Text] [Related]  

  • 28. [The absence of uniparental X-chromosome inheritance in spontaneous abortuses with a 46,XX karyotype].
    Evdokimova VN; Nazarenko SA
    Ontogenez; 2000; 31(3):201-4. PubMed ID: 10867934
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Epigenetic effects of trisomy 16 in the human placenta].
    Tolmacheva EN; Kashevarova AA; Skriabin NA; Lebedev IN
    Mol Biol (Mosk); 2013; 47(3):423-32. PubMed ID: 23888773
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.
    Beever CL; Stephenson MD; Peñaherrera MS; Jiang RH; Kalousek DK; Hayden M; Field L; Brown CJ; Robinson WP
    Am J Hum Genet; 2003 Feb; 72(2):399-407. PubMed ID: 12497247
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
    Lose F; Duffy DL; Kay GF; Kedda MA; Spurdle AB; ;
    J Natl Cancer Inst; 2008 Nov; 100(21):1519-29. PubMed ID: 18957670
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Epigenetic inactivation of the RB1 gene as a factor of genomic instability: a possible contribution to etiology of chromosomal mosaicism during human embryo development].
    Tolmacheva EN; Kashevarova AA; Sukhanova NN; Sazhenova EA; Lebedev IN
    Genetika; 2008 Nov; 44(11):1461-7. PubMed ID: 19137728
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.
    Ozcelik T; Uz E; Akyerli CB; Bagislar S; Mustafa CA; Gursoy A; Akarsu N; Toruner G; Kamel N; Gullu S
    Eur J Hum Genet; 2006 Jun; 14(6):791-7. PubMed ID: 16596118
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy.
    Yong PJ; McFadden DE; Robinson WP
    J Obstet Gynaecol Can; 2012 Dec; 34(12):1141-1148. PubMed ID: 23231796
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.
    Lanasa MC; Hogge WA; Kubik CJ; Ness RB; Harger J; Nagel T; Prosen T; Markovic N; Hoffman EP
    Am J Obstet Gynecol; 2001 Sep; 185(3):563-8. PubMed ID: 11568778
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.
    Markovic VD; Chitayat DA; Ritchie SM; Chodakowski BA; Hutton EM
    Am J Med Genet; 1996 Feb; 61(4):363-70. PubMed ID: 8834049
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion.
    Bagislar S; Ustuner I; Cengiz B; Soylemez F; Akyerli CB; Ceylaner S; Ceylaner G; Acar A; Ozcelik T
    Aust N Z J Obstet Gynaecol; 2006 Oct; 46(5):384-7. PubMed ID: 16953851
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Analysis of non-disjunction in human trisomic spontaneous abortions.
    Hassold TJ; Takaesu N
    Prog Clin Biol Res; 1989; 311():115-34. PubMed ID: 2570425
    [No Abstract]   [Full Text] [Related]  

  • 39. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK; Hardin EL; Pacheco C; Kuslich CD; Donlon TA
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.
    Hansson K; Poelma WM; Zondervan HA; Leschot NJ
    Prenat Diagn; 1998 Sep; 18(9):975-8. PubMed ID: 9793985
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.