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 *

129 related articles for article (PubMed ID: 5808536)

  • 1. Enlarged satellites and other variants of chromosome structure in a Swiss family.
    Yunibhand P
    J Genet Hum; 1969 May; 17(1):115-26. PubMed ID: 5808536
    [No Abstract]   [Full Text] [Related]  

  • 2. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
    Haberlandt W
    Arztl Forsch; 1971 Jul; 25(7):218-23. PubMed ID: 5109598
    [No Abstract]   [Full Text] [Related]  

  • 3. [Familial inversions and other concomitant chromosome aberrations].
    Catti A
    J Genet Hum; 1975 Oct; 23 SUPPL():92-5. PubMed ID: 1214174
    [No Abstract]   [Full Text] [Related]  

  • 4. Chromosome mapping of the Duffy blood group locus.
    Pergament E; Rowley JD; Kadotani T; Sato H; Berlow S
    Chic Med Sch Q; 1968; 27(4):216-21. PubMed ID: 5742686
    [No Abstract]   [Full Text] [Related]  

  • 5. A new case of human Y chromosome with satellites on the long arm.
    Stella M; Rossi R; Bonfante A; Rossi G
    J Genet Hum; 1980 Mar; 28(1):39-45. PubMed ID: 7190602
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Deafness and anomalies of the lacrimal duct in a family with translocation t(17;22)].
    Ballesta F; Hernandez JV
    J Genet Hum; 1976 Nov; 24 Suppl():221-5. PubMed ID: 1025274
    [No Abstract]   [Full Text] [Related]  

  • 8. [A new observation of chromosome aberrations 18p].
    De Grouchy J; Rossier A; Joab N
    Ann Genet; 1967 Dec; 10(4):221-3. PubMed ID: 5302448
    [No Abstract]   [Full Text] [Related]  

  • 9. A study of chromosomes in couples with habitual abortions.
    Kyaosaar ME
    Sov Genet; 1974 Mar; 7(12):1600-3. PubMed ID: 4827771
    [No Abstract]   [Full Text] [Related]  

  • 10. [RV polymorphism of the chromosomes in newborn infants].
    Krachunova M; Tsancheva M; Lozanova T
    Eksp Med Morfol; 1980; 19(3):144-8. PubMed ID: 7418645
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome studies of a family with an abnormally large Y chromosome.
    Sugahara T; Sakurai M
    Jinrui Idengaku Zasshi; 1967 Dec; 12(3):190-6. PubMed ID: 5626879
    [No Abstract]   [Full Text] [Related]  

  • 12. [18p- syndrome. A further case].
    Ayraud N; Darcourt G; D'Oelsnitz M; Poujol J; Lavagna J; Capdeville C
    Ann Genet; 1969 Jun; 12(2):122-5. PubMed ID: 5308384
    [No 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. Pericentric Y-inversion.
    Nielsen J; Rasmussen J
    J Genet Hum; 1974 Mar; 22(1):21-9. PubMed ID: 4430896
    [No Abstract]   [Full Text] [Related]  

  • 15. [A recent case of partial deletion of short arm of chromosome 18].
    Vaillaud JC; Martin J; Ayraud N
    Ann Genet; 1970 Jun; 13(2):120-2. PubMed ID: 5310694
    [No Abstract]   [Full Text] [Related]  

  • 16. Human chromosome fluorescence.
    Borganokar DS; McKusick VA
    Johns Hopkins Med J; 1971 Feb; 128(2):75-8. PubMed ID: 5551931
    [No Abstract]   [Full Text] [Related]  

  • 17. Y chromosome duplication in chronic myeloid leukemia.
    Stoll C; Oberling F
    Nouv Rev Fr Hematol (1978); 1982; 24(1):9-12. PubMed ID: 6951142
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Human chromosomal polymorphism and reproductive function disorder. III. Extreme autosomal C-variants: an analysis of their distribution and combination in the karyotype].
    Tsetkova TG
    Genetika; 1980; 16(12):2210-6. PubMed ID: 7194831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ring chromosome 21 in a normal female.
    Kleczkowska A; Fryns JP
    Ann Genet; 1984; 27(2):126-8. PubMed ID: 6331791
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Rare structural rearrangement of the Y chromosome (Yq-,S) in the family of a boy with a sex differentiation disorder].
    Verlinskaia DK; Kovaleva NV; Prozorova MV; Khitrikova LE
    Tsitologiia; 1983 Feb; 25(2):204-6. PubMed ID: 6134363
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.