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 *

106 related articles for article (PubMed ID: 5058917)

  • 1. [Monosomy for the centromeric regions of chromosome 21].
    Rethoré MO; Dutrillaux B; Baheux G; Gerveaux J; Lejeune J
    Exp Cell Res; 1972 Feb; 70(2):455-6. PubMed ID: 5058917
    [No Abstract]   [Full Text] [Related]  

  • 2. [Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation].
    Lejeune J; Rethore MO; Dutrillaux B; Martin G
    Exp Cell Res; 1972 Sep; 74(1):293-5. PubMed ID: 5073314
    [No Abstract]   [Full Text] [Related]  

  • 3. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M; Schmid E; Röttinger E
    Humangenetik; 1968; 6(4):303-10. PubMed ID: 5713616
    [No Abstract]   [Full Text] [Related]  

  • 4. Monosomy for the centromeric and juxtacentromeric region of chromosome 21.
    Holbek S; Friedrich U; Brostrom K; Petersen GB
    Humangenetik; 1974; 24(3):191-5. PubMed ID: 4140831
    [No Abstract]   [Full Text] [Related]  

  • 5. [Trisomy of the short arm of 9 with isochromosome 9p and partial monosomy Yq].
    Geneix A; Jaffray JY; Charbonne F; Perissel B; Malpuech G; Malet P; Roland MO
    Ann Genet; 1983; 26(2):103-5. PubMed ID: 6604482
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case of annular chromosome 9. Indentification by controlled denaturation].
    Fraisse J; Lauras B; Ooghe MJ; Freycon F; Rethoré MO
    Ann Genet; 1974 Sep; 17(3):175-80. PubMed ID: 4548818
    [No Abstract]   [Full Text] [Related]  

  • 7. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H; Rivas F; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Identification of human G chromosomes by the denaturation technique].
    Dutrillaux B; Rethoré MO; Prieur M; Raoul O; Berger R; Lejeune J
    Exp Cell Res; 1972 Feb; 70(2):453-5. PubMed ID: 4110307
    [No Abstract]   [Full Text] [Related]  

  • 9. Monosomy G: case report and review of the literature.
    Greenwood RD; Sommer A
    J Med Genet; 1971 Dec; 8(4):496-500. PubMed ID: 5149533
    [No Abstract]   [Full Text] [Related]  

  • 10. Autosomal monosomy (45, XX, C--) in a human embryo with total amelia and further malformations.
    Pawlowitzki IH; Cenani A; Frischibier HJ
    Clin Genet; 1973; 4(3):193-202. PubMed ID: 4765202
    [No Abstract]   [Full Text] [Related]  

  • 11. [Autosomal chromosome aberrations].
    Schinzel A
    Arch Genet (Zur); 1979; 52(1-2):1-204. PubMed ID: 389192
    [No Abstract]   [Full Text] [Related]  

  • 12. [Autosomal chromosome aberrations].
    Serville F; Battin J
    Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
    [No Abstract]   [Full Text] [Related]  

  • 13. Complex structural rearrangement of chromosomes 7, 10, 14 and 21.
    de Asis ML; Saito F; Tonomura A
    Jinrui Idengaku Zasshi; 1984 Dec; 29(4):453-9. PubMed ID: 6535858
    [No Abstract]   [Full Text] [Related]  

  • 14. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Full monosomy 21: a clinically recognizable syndrome?
    Fryns JP; D'Hondt F; Goddeeris P; van den Berghe H
    Hum Genet; 1977 Jun; 37(2):155-9. PubMed ID: 885536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Chromosome aberrations in abortions].
    Boué JG; Boué A; Lazar P
    Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690
    [No Abstract]   [Full Text] [Related]  

  • 17. [Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].
    Tenconi R; Baccichetti C; Dussini N; Panizza G
    Ann Genet; 1974 Dec; 17(4):275-7. PubMed ID: 4281288
    [No Abstract]   [Full Text] [Related]  

  • 18. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH; Bobrow M
    J Med Genet; 1975 Mar; 12(1):29-43. PubMed ID: 123589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 20. Chromosome abnormalities in human leukemia.
    Rowley JD
    Annu Rev Genet; 1980; 14():17-39. PubMed ID: 7011172
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.