These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 592356)

  • 21. Jumping translocations in spontaneous abortions.
    Levy B; Dunn TM; Hirschhorn K; Kardon N
    Cytogenet Cell Genet; 2000; 88(1-2):25-9. PubMed ID: 10773659
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Centromere Destiny in Dicentric Chromosomes: New Insights from the Evolution of Human Chromosome 2 Ancestral Centromeric Region.
    Chiatante G; Giannuzzi G; Calabrese FM; Eichler EE; Ventura M
    Mol Biol Evol; 2017 Jul; 34(7):1669-1681. PubMed ID: 28333343
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Antenatal diagnosis of Patau's syndrome (trisomy 13) including a detailed pathological study of the fetus.
    Butler LJ; Reiss HE; France NE; Briddon S
    J Med Genet; 1973 Dec; 10(4):367-70. PubMed ID: 4129972
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal karyotype analysis in high risk families.
    Aula P; Karjalainen O
    Ann Clin Res; 1973 Jun; 5(3):142-8. PubMed ID: 4127164
    [No Abstract]   [Full Text] [Related]  

  • 25. Centromeric association of chromosome 16- and 18-derived microchromosomes.
    Felbor U; Rutschow D; Haaf T; Schmid M
    Hum Genet; 2002 Jul; 111(1):16-25. PubMed ID: 12136231
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A new stable human dicentric chromosome, tdic(4;21)(p16;q22), in a woman with first trimester abortion.
    Wang F; Li Y
    J Med Genet; 1993 Aug; 30(8):696. PubMed ID: 8411059
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.
    Ebbin AJ; Wilson MG; Towner JW; Slaughter JP
    J Med Genet; 1973 Mar; 10(1):65-9. PubMed ID: 4697854
    [TBL] [Abstract][Full Text] [Related]  

  • 28. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
    Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
    Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Switching the centromeres on and off: epigenetic chromatin alterations provide plasticity in centromere activity stabilizing aberrant dicentric chromosomes.
    Sato H; Saitoh S
    Biochem Soc Trans; 2013 Dec; 41(6):1648-53. PubMed ID: 24256269
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The fate of DNA satellites I, II, III and ribosomal DNA in a familial dicentric chromosome 13:14.
    Gosden JR; Gosden C; Lawrie S; Mitchell AR
    Hum Genet; 1978 Mar; 41(2):131-41. PubMed ID: 640652
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia.
    Fass B; Kaplan S; Lippe B; Sparkes RS
    J Med Genet; 1978 Jun; 15(3):232-6. PubMed ID: 671491
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.
    Mackinnon RN; Campbell LJ
    Cytogenet Genome Res; 2007; 119(3-4):211-20. PubMed ID: 18253031
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves.
    Sumner AT; Mitchell AR; Ellis PM
    J Med Genet; 1998 Oct; 35(10):833-5. PubMed ID: 9783707
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Satellited 4q identified in amniotic fluid cells.
    Miller I; Songster G; Fontana S; Hsieh CL
    Am J Med Genet; 1995 Jan; 55(2):237-9. PubMed ID: 7717425
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chromosome segregation, kinetochores and DNA-microtubule interaction: a preferential satellite DNA-MAP interaction may be conserved in evolution.
    Marx KA; Denial T
    Prog Clin Biol Res; 1985; 172B():65-75. PubMed ID: 3991723
    [No Abstract]   [Full Text] [Related]  

  • 36. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chromosomal mosaicism in amniotic cell culture. A diagnostic Dilemma.
    Kohn G; Mennuti MT; Kaback M; Schwartz RM; Chemke J; Goldman B; Mellman WJ
    Isr J Med Sci; 1975 May; 11(5):476-81. PubMed ID: 1158661
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Structure and inheritance of some heterozygous Robertsonian translocation in man.
    Daniel A; Lam-Po-Tang PR
    J Med Genet; 1976 Oct; 13(5):381-8. PubMed ID: 1003449
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.
    Wevrick R; Willard HF
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9394-8. PubMed ID: 2594775
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Relationship of mouse minor satellite DNA to centromere activity.
    Broccoli D; Miller OJ; Miller DA
    Cytogenet Cell Genet; 1990; 54(3-4):182-6. PubMed ID: 2265565
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.