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 *

261 related articles for article (PubMed ID: 6460476)

  • 1. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.
    MacFaul R; Turner T; Mason MK
    Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.
    Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV
    Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425
    [No Abstract]   [Full Text] [Related]  

  • 3. Prenatal diagnosis of trisomy 21 and X/XX sex chromosome mosaicism.
    McCorquodale MM; Cummins T; Furlong J
    Prenat Diagn; 1985; 5(4):295-8. PubMed ID: 2931678
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
    Grosse KP; Hopfengärtner F; Schwanitz G
    Humangenetik; 1971; 13(4):333-7. PubMed ID: 4257570
    [No Abstract]   [Full Text] [Related]  

  • 6. Double aneuploidy. Turner-Down syndrome.
    Townes PL; White MR; Stiffler SJ; Goh K
    Am J Dis Child; 1975 Sep; 129(9):1062-5. PubMed ID: 127528
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A report of 2 cases of Turner's syndrome with a ring X chromosome].
    Migliori MV; Bartolotta E; Maurizi M; Bonazzi P; Cardinale G; Manunza V
    Minerva Pediatr; 1991 Sep; 43(9):605-9. PubMed ID: 1758399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Undetected sex chromosome aneuploidy by chromosomal microarray.
    Markus-Bustani K; Yaron Y; Goldstein M; Orr-Urtreger A; Ben-Shachar S
    Prenat Diagn; 2012 Nov; 32(11):1117-8. PubMed ID: 23034780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic evaluation of fetal death: the role of amniocentesis.
    Saal HM; Rodis J; Weinbaum PJ; DiMaggio R; Landrey TM
    Obstet Gynecol; 1987 Oct; 70(4):601-3. PubMed ID: 2957622
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Confirmation of prenatal diagnosis of sex chromosome mosaicism.
    McFadden DE; Kalousek DK
    Am J Med Genet; 1989 Apr; 32(4):495-7. PubMed ID: 2773991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A case of maternal 45,X/46,XX mosaicism detected by non-invasive prenatal testing].
    Tian Y; Zhang L; Tian W; Wu Y; Zheng Q; Zhang Z; Jia L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov; 36(11):1120-1122. PubMed ID: 31703140
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Double trisomy as a mosaic. Case history (48, XYY, + 21/47,XY, +21) and survey of the literature of mixed autosomal-gonosomal trisomies.
    Schwanitz G; Hagner M
    Acta Genet Med Gemellol (Roma); 1978; 27():67-74. PubMed ID: 155969
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R; Pfeiffer RA; Kollert A; Beinder E
    Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sex chromosome mosaicism not detected at amniocentesis.
    Roland B; Cox DM; Rudd NL
    Prenat Diagn; 1990 May; 10(5):333-6. PubMed ID: 2143821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40-year-old woman with a mosaic Turner's karyotype (45,X/47,XXX).
    Acharya G; Jonsrud C; van der Hagen C; Maltau JM
    Acta Obstet Gynecol Scand; 2003 Aug; 82(8):773-4. PubMed ID: 12848653
    [No Abstract]   [Full Text] [Related]  

  • 17. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW; Haar BG; Scheres JM; Rutten FJ
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract]   [Full Text] [Related]  

  • 18. Fertility in women with Turner's syndrome. Case report and review of literature.
    Nielsen J; Sillesen I; Hansen KB
    Br J Obstet Gynaecol; 1979 Nov; 86(11):833-5. PubMed ID: 508669
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Double aneuploidy with Down's-Klinefelter's syndrome.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Apr; 95(4):350-2. PubMed ID: 8935309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal screening for Down's syndrome with use of maternal serum markers.
    Haddow JE; Palomaki GE; Knight GJ; Williams J; Pulkkinen A; Canick JA; Saller DN; Bowers GB
    N Engl J Med; 1992 Aug; 327(9):588-93. PubMed ID: 1379344
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.