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 *

127 related articles for article (PubMed ID: 1438065)

  • 1. Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, idic(Yp).
    Bernstein R; Steinhaus KA; Cain MJ
    Prenat Diagn; 1992 Sep; 12(9):709-16. PubMed ID: 1438065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal identification of an isochromosome for the short arm of the Y i(Yp), by cytogenetic and molecular analyses.
    Slim R; Soulié J; Hotmar J; Lecolier B; Bercau G; Bernheim A
    Prenat Diagn; 1994 Jan; 14(1):23-8. PubMed ID: 8183834
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
    Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line.
    Chen CP; Chern SR; Chen SW; Wu FT; Lee CC; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 May; 61(3):528-531. PubMed ID: 35595452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Y isochromosome associated with a mosaic karyotype and inactivation of the centromere.
    Haaf T; Schmid M
    Hum Genet; 1990 Oct; 85(5):486-90. PubMed ID: 2227931
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cytogenetic characterization of an isodicentric Yq and a neocentric isochromosome Yp in an azoospermic male.
    Jiang Y; Yue F; Wang R; Zhang H; Li L; Li L; Li S; Liu R
    Mol Med Rep; 2020 Feb; 21(2):918-926. PubMed ID: 31974623
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.
    Zheng J; Yang X; Lu H; Guan Y; Yang F; Xu M; Li M; Ji X; Wang Y; Hu P; Zhou Y
    Mol Med Rep; 2019 Mar; 19(3):1791-1796. PubMed ID: 30592288
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fluorescent in-situ hybridization (FISH) as an aid to marker chromosome identification in prenatal diagnosis.
    Amiel A; Fejgin M; Appelman Z; Shapiro I; Gaber E; Bachar A; Zamir R; Kedar I; Golbus M
    Eur J Obstet Gynecol Reprod Biol; 1995 Mar; 59(1):103-7. PubMed ID: 7781851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal investigation of a 45,X/46,X,r(?) karyotype in amniocytes using fluorescence in situ hybridization with an X-centromeric probe.
    Bajalica S; Bui TH; Koch J; Bröndum-Nielsen K
    Prenat Diagn; 1992 Jan; 12(1):61-4. PubMed ID: 1557312
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rapid identification of marker chromosomes using primed in situ labeling (PRINS).
    Velagaleti GV; Tharapel SA; Martens PR; Tharapel AT
    Am J Med Genet; 1997 Aug; 71(2):130-3. PubMed ID: 9217209
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis.
    Verschraegen-Spae MR; van Roy N; de Perdigo A; de Paepe A; Speleman F
    Prenat Diagn; 1993 May; 13(5):385-94. PubMed ID: 8341637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Lai ST; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A; Blanco B; del Castillo V; Carnevale A
    Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations.
    Huang B; Thangavelu M; Bhatt S; J Sandlin C; Wang S
    Prenat Diagn; 2002 Feb; 22(2):105-10. PubMed ID: 11857613
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
    Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification.
    Lin SY; Lee CN; Peng AY; Yuan TJ; Lee DJ; Lin WH; Ma GC; Chen M
    J Formos Med Assoc; 2018 Nov; 117(11):1027-1031. PubMed ID: 29752043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.
    Lebo RV; Milunsky J; Higgins AW; Loose B; Huang XL; Wyandt HE
    Am J Med Genet; 1999 Aug; 85(5):429-37. PubMed ID: 10405438
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.