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 *

74 related articles for article (PubMed ID: 5399209)

  • 1. Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.
    Brogger A
    Hereditas; 1969; 62(1):116-30. PubMed ID: 5399209
    [No Abstract]   [Full Text] [Related]  

  • 2. [A short arm deletion of chromosome 13].
    Emerit I; de Grouchy J; German J
    Ann Genet; 1968 Sep; 11(3):184-6. PubMed ID: 5304619
    [No Abstract]   [Full Text] [Related]  

  • 3. [Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)].
    de Grouchy J; Crippa L; German J
    Ann Genet; 1970 Mar; 13(1):19-37. PubMed ID: 5310103
    [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. Short arm deletion of chromosome 14.
    Emerit I; Noel B; Thiriet M; Loubon M; Quack B
    Humangenetik; 1972; 15(1):33-8. PubMed ID: 5046906
    [No Abstract]   [Full Text] [Related]  

  • 6. Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.
    Ferguson-Smith MA; Newman BF; Ellis PM; Thomson DM; Riley ID
    Nat New Biol; 1973 Jun; 243(130):271-4. PubMed ID: 4515493
    [No Abstract]   [Full Text] [Related]  

  • 7. Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p).
    Palmer CG; Conneally PM; Christian JC
    J Med Genet; 1969 Jun; 6(2):166-73. PubMed ID: 4240722
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Chronology and pattern of human chromosome replication. X. Autoradiographic studies of an abnormal familial chromosome of the D (13-15) group.
    Hossfeld DK; Ikeuchi T; Sandberg AA
    Cytogenetics; 1970; 9(5):351-9. PubMed ID: 5501392
    [No Abstract]   [Full Text] [Related]  

  • 10. Meiotic consequences of pericentric inversions of chromosome 13.
    Wenger SL; Steele MW
    Am J Med Genet; 1981; 9(4):275-83. PubMed ID: 7294066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)].
    Tolksdorf M; Goll U; Wiedemann HR; Pfeiffer RA
    Arch Kinderheilkd; 1970; 181(3):282-95. PubMed ID: 5488682
    [No Abstract]   [Full Text] [Related]  

  • 12. Gene mapping by exclusion: the current status.
    Aitken DA; Ferguson-Smith MA; Dick HM
    Birth Defects Orig Artic Ser; 1976; 12(7):256-65. PubMed ID: 1024621
    [No Abstract]   [Full Text] [Related]  

  • 13. Duplication of the distal segment of 14q.
    Atkin JF; Patil S
    Am J Med Genet; 1983 Nov; 16(3):357-66. PubMed ID: 6196971
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Demonstration of two regions involved in chromosome 1p deletion in breast tumors].
    Bièche I; Champème MH; Matifas F; Cropp C; Callahan R; Lidereau R
    Bull Cancer; 1994 Feb; 81(2):108-13. PubMed ID: 7894115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A human chromosome translocation from the eighteenth century].
    Stalder GR; Bühler EM
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1967; 41(2-4):87-93. PubMed ID: 5631509
    [No Abstract]   [Full Text] [Related]  

  • 16. [Method of analysis of asynchronism of chromosome replication at the end of the S period].
    Podugol'nikova OA; Korostelev AP
    Tsitologiia; 1974 Aug; 16(8):1041-5. PubMed ID: 4420838
    [No Abstract]   [Full Text] [Related]  

  • 17. Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.
    Magenis RE; Koler RD; Lovrien E; Bigley RH; DuVal MC; Overton KM
    Proc Natl Acad Sci U S A; 1975 Nov; 72(11):4526-30. PubMed ID: 1060135
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
    Magenis RE; Koler RD; Lovrien E; Bigley RH; DuVal MC; Overton KM
    Birth Defects Orig Artic Ser; 1976; 12(7):326-7. PubMed ID: 1024633
    [No Abstract]   [Full Text] [Related]  

  • 19. Inherited 13/14 chromosome translocation as a cause of human fetal wastage.
    Sparkes RS; De Chieri PR
    Obstet Gynecol; 1970 Apr; 35(4):601-7. PubMed ID: 5438152
    [No Abstract]   [Full Text] [Related]  

  • 20. Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
    Gibas Z; Prout GR; Connolly JG; Pontes JE; Sandberg AA
    Cancer Res; 1984 Mar; 44(3):1257-64. PubMed ID: 6692407
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.