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 *

300 related articles for article (PubMed ID: 127528)

  • 1. 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]  

  • 2. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
    Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA
    Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic survey of 504 mentally retarded individuals.
    Singh DN; Osborne RA; Paul JR; Catoe S; Katzberg A; Hennigar GR; Barnett CD
    J Ment Defic Res; 1974 Dec; 18(4):293-305. PubMed ID: 4282744
    [No Abstract]   [Full Text] [Related]  

  • 5. An infant with Turner-Down aneuploidy and massive capillary hemangioma of the orbit: a case report with review.
    Musarella MA; Verma RS
    Ann Genet; 2001; 44(2):67-70. PubMed ID: 11522243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Mosaic double aneuploidy of X and G chromosomes.
    Osborne RA; Hennigar GR; Barnett CD
    Am J Ment Defic; 1975 May; 79(6):644-7. PubMed ID: 125038
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An infant with Down-Turner double aneuploidy: a case report and literature review.
    Jaruratanasirikul S; Jinorose U
    J Med Assoc Thai; 1995 Feb; 78(2):108-12. PubMed ID: 7629445
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Indications for chromosome analysis from the pediatric viewpoint].
    Steinbicker V; Braun HS; Hemke G; Euchler HB
    Kinderarztl Prax; 1973 Feb; 41(2):91-8. PubMed ID: 4267824
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Results of 538 chromosome studies on patients referred for cytogenetic analysis.
    Mulcahy MT; Jenkyn J
    Med J Aust; 1972 Dec; 2(24):1333-8. PubMed ID: 4265391
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Multiple marker screening test: identification of fetal cystic hygroma, hydrops, and sex chromosome aneuploidy.
    Wenstrom KD; Boots LR; Cosper PC
    J Matern Fetal Med; 1996; 5(1):31-5. PubMed ID: 8796763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Turner syndrome and 45,X/47,XXX mosaicism.
    Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
    Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [The chromosomal syndromes (author's transl)].
    Klein D
    Padiatr Padol Suppl; 1975; 4():1-31. PubMed ID: 127145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+21.
    Costa GRC; Jorente J; Pontes LB; Viguetti Campos NL; Marques-de-Faria AP; Vieira TP; Steiner CE
    Cytogenet Genome Res; 2024; 164(2):103-109. PubMed ID: 39068925
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mosaic cell lines, or leucocyte culturing anomalies?
    Keeler C
    J Hered; 1973; 64(3):167-8. PubMed ID: 4745490
    [No Abstract]   [Full Text] [Related]  

  • 19. Mosaic double aneuploidy (45,X/47,XX,+8) with aortic dissection.
    Lee MN; Choi KH; Kim DK; Kim SH
    Genet Couns; 2014; 25(2):177-82. PubMed ID: 25059016
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal conditions in congenital heart disease.
    Dahl G
    Acta Paediatr Scand; 1970 Jan; 59(1):65-73. PubMed ID: 4247306
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.