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 *

102 related articles for article (PubMed ID: 19161142)

  • 1. Identification of sex chromosome mosaicism: is analysis of 20 metaphase cells sufficient?
    Wiktor AE; Bender G; Van Dyke DL
    Am J Med Genet A; 2009 Feb; 149A(2):257-9. PubMed ID: 19161142
    [No Abstract]   [Full Text] [Related]  

  • 2. CYTOGENETIC STUDIES OF TWO PATIENTS WITH XXX-XX-XO AND XY-XO MOSAICISM.
    WU M; PAN HJ; CHAN PK; SHAO HH
    Chin Med J; 1964 Feb; 83():80-8. PubMed ID: 14140012
    [No Abstract]   [Full Text] [Related]  

  • 3. Cytogenetic analysis and reporting.
    Campbell LJ
    Methods Mol Biol; 2011; 730():259-68. PubMed ID: 21431647
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Revised guidelines for the diagnosis of mosaicism in amniocytes.
    Hsu LY; Benn PA
    Prenat Diagn; 1999 Nov; 19(11):1081-82. PubMed ID: 10589067
    [No Abstract]   [Full Text] [Related]  

  • 5. Detection of the fragile X chromosome and other fragile sites.
    Hecht F; Sutherland GR
    Clin Genet; 1984 Oct; 26(4):301-3. PubMed ID: 6499245
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Quality control in components of comparative genomic hybridization technique used for diagnostic cytogenetic analysis.
    Loukianova TA; Tang SS; Kalousek DK
    Prenat Diagn; 2000 Dec; 20(12):1019. PubMed ID: 11113920
    [No Abstract]   [Full Text] [Related]  

  • 7. [The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome].
    Barros BA; Maciel-Guerra AT; De Mello MP; Coeli FB; Carvalho AB; Viguetti-Campos N; Assumpção Jde G; Marques-de-Faria AP; Lemos-Marini SH; Guerra-Junior G
    Arq Bras Endocrinol Metabol; 2009 Dec; 53(9):1137-42. PubMed ID: 20126871
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis.
    Wyandt HE; Tonk VS; Huang XL; Evans AT; Milunsky JM; Milunsky A
    Fetal Diagn Ther; 2006; 21(2):235-40. PubMed ID: 16491010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cytogenetic characterization of two small supernumerary marker chromosomes derived from chromosome 19.
    Dennis TR; Raptoulis GN; Stalker HJ; Boles D; Meck JM; Krasnewich DM; Schiffmann R; Zori RT
    Am J Med Genet A; 2009 Feb; 149A(2):262-5. PubMed ID: 19133694
    [No Abstract]   [Full Text] [Related]  

  • 10. Characterization of a supernumerary ring chromosome 1 mosaicism in two cell systems by molecular cytogenetic techniques and review of the literature.
    Tönnies H; Neumann LM; Grüneberg B; Neitzel H
    Am J Med Genet A; 2003 Aug; 121A(2):163-7. PubMed ID: 12910498
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical manifestation and cytogenetic analysis of 607 patients with Turner syndrome].
    Zheng J; Liu Z; Xia P; Lai Y; Wei Y; Liu Y; Chen J; Qin L; Xie L; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):61-64. PubMed ID: 28186596
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic follow-up of chromosomal mosaicism detected in first-trimester prenatal diagnosis.
    Battaglia P; Baroncini A; Mattarozzi A; Baccolini I; Capucci A; Spada F; Pompilii E; Pittalis MC
    Prenat Diagn; 2014 Aug; 34(8):739-47. PubMed ID: 24633594
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].
    Romana SP; Gosset P; Elghezal H; Le Lorc'h M; Ozilou C; Lapierre JM; Sanlaville D; Brisset S; Turleau C; Vekemans M
    J Gynecol Obstet Biol Reprod (Paris); 2001 Feb; 30(1 Suppl):75-9. PubMed ID: 11240520
    [No Abstract]   [Full Text] [Related]  

  • 14. An external quality assessment scheme for prenatal detection of rare chromosomal abnormalities.
    Weng B; Li X
    Clin Chim Acta; 2012 Nov; 413(21-22):1721-4. PubMed ID: 22789962
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal mosaicism in the fetoplacental unit.
    Grati FR; Malvestiti F; Branca L; Agrati C; Maggi F; Simoni G
    Best Pract Res Clin Obstet Gynaecol; 2017 Jul; 42():39-52. PubMed ID: 28284509
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disorder of sex development in a cat with chromosome mosaicism 37,X/38,X,r(Y).
    Szczerbal I; Stachowiak M; Nowacka-Woszuk J; Dzimira S; Szczepanska K; Switonski M
    Reprod Domest Anim; 2017 Oct; 52(5):914-917. PubMed ID: 28370681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome aberrations identified by cytogenetic analysis of the first two clones of cultured amniotic fluid cells compared with QF-PCR results.
    Jenderny J; Schmidt W; Kochhan L
    Cytogenet Genome Res; 2014; 142(4):239-44. PubMed ID: 24853086
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sex chromosome mosaicism in couples undergoing intracytoplasmic sperm injection.
    Morel F; Gallon F; Amice V; Le Bris MJ; Le Martelot MT; Roche S; Valéri A; Derrien V; Herry A; Amice J; De Braekeleer M
    Hum Reprod; 2002 Oct; 17(10):2552-5. PubMed ID: 12351527
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mixed gonadal dysgenesis and sex chromosome mosaicism with multiple cell lines including structural aberrations of the Y chromosome.
    Al-Awadi SA; Cuschieri A; Farag TI; Naguib K; Teebi AS; Issa M; El-Sayed M
    Clin Genet; 1983 Feb; 23(2):172-6. PubMed ID: 6682358
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Three cases of sex chromosome mosaicism with a nonfluorescent Y.
    Madan K; Gooren L; Schoemaker J
    Hum Genet; 1979 Feb; 46(3):295-304. PubMed ID: 437772
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.