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 *

241 related articles for article (PubMed ID: 59989)

  • 1. [Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite].
    Kulikov RI; Mashkova MV; Verlinskaia DK; Bondarev GN
    Tsitologiia; 1976 Feb; 18(2):213-8. PubMed ID: 59989
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Updating advances in cytogenetics. Applications of the new chromosome banding methods.
    Breg WR
    Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402
    [No Abstract]   [Full Text] [Related]  

  • 3. Non-fluorescent Y-chromosome.
    Bühler EM; Bühler UK; Tsuchimoto T; Stalder GR
    Helv Paediatr Acta; 1974 Nov; 29(5):447-56. PubMed ID: 4141700
    [No Abstract]   [Full Text] [Related]  

  • 4. Developments in laboratory diagnosis of chromosomal abnormalities.
    Frias JL
    Ann Clin Lab Sci; 1975; 5(5):369-76. PubMed ID: 52330
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Value of the use of fluorescent substances in the study of normal and pathologic human karyotypes. I. Identification of the Y chromosome].
    Franceschini P; Fabris C; Bogetti G; Santoro MA; Chaippo G
    Minerva Pediatr; 1972 Jun; 24(21):862-7. PubMed ID: 4114776
    [No Abstract]   [Full Text] [Related]  

  • 6. The use of fluorescence techniques for the recognition of mammalian chromosomes and chromosome regions.
    Caspersson T; Lindsten J; Lomakka G; Moller A; Zech L
    Int Rev Exp Pathol; 1972; 11():1-72. PubMed ID: 4122097
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. 45,X/46,X,dic(Yq) mosaicism and mixed gonadal dysgenesis. Case report and review of the literature.
    Armandares S; Salamanca F; Cos J; Chavarria C
    Ann Genet; 1977 Dec; 20(4):269-72. PubMed ID: 305755
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dicentric Y chromosome in mixed gonadal dysgenesis.
    Hayek A; Yunis E
    J Med Genet; 1975 Jun; 12(2):210-2. PubMed ID: 49429
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human chromosome analysis.
    Centerwall WR; Murdoch JL
    Am Fam Physician; 1975 Apr; 11(4):76-89. PubMed ID: 123406
    [No Abstract]   [Full Text] [Related]  

  • 11. [Effect of the Y chromosome on the morphology of human F-chromatin under normal and pathological conditions].
    Kulikov RI
    Tsitologiia; 1977 Jul; 19(7):732-8. PubMed ID: 73242
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sex chromosome mosaicism of X/XY or X/XY/XYY.
    Wilson MG; Ebbin AJ; Shinno NW; Towner JW
    Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].
    Malpuech G; Raynaud EJ; Belin J; Godeneche P; de Grouchy J
    Ann Genet; 1971 Sep; 14(3):213-8. PubMed ID: 5315468
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
    del Solar C; Uchida IA
    J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
    [No Abstract]   [Full Text] [Related]  

  • 15. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome].
    Verlinskaia DK; Prozorova MV
    Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.
    Caspersson T; Hultén M; Jonasson J; Lindsten J; Therkelsen A; Zech L
    Hereditas; 1971; 68(2):317-24. PubMed ID: 4142012
    [No Abstract]   [Full Text] [Related]  

  • 17. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L; Jackson J; Cowell C; Sillence D; Smith A
    Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Fluorescence microscopy of Y chromatin. A method for the study of Y-chromosome abnormalities].
    Nielsen H; Skakkebaek NE; Philip J
    Ugeskr Laeger; 1971 Apr; 133(14):631-4. PubMed ID: 4102670
    [No Abstract]   [Full Text] [Related]  

  • 19. Laparoscopy in endocrine and genetic disorders of the gonads.
    Minozzi M; Faggiano M; Jori GP; Lombardi G
    Acta Endocrinol Suppl (Copenh); 1975; 192():1-124. PubMed ID: 123111
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.