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 *

50 related articles for article (PubMed ID: 4349854)

  • 1. [Combination of the Rh-deletion type and silent Fy-gene].
    Schleyer F; Spielmann W; Oepen I
    Beitr Gerichtl Med; 1973; 30():389-93. PubMed ID: 4349854
    [No Abstract]   [Full Text] [Related]  

  • 2. [Rh-defect types, their diagnosis and significance].
    Spielmann W
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1971; 96(3):369-79. PubMed ID: 4111761
    [No Abstract]   [Full Text] [Related]  

  • 3. [The forensic significance of the "silent" gene Su (observation of Su in three generations) (author's transl)].
    Speiser P; Pausch V
    Wien Klin Wochenschr; 1981 Apr; 93(7):221-3. PubMed ID: 7257416
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Usefulness of evaluating the probability of homozygotism with regard to the Dd features of the Rh system in the father in comparison with the homozygotism of the child in cases of disputed paternity].
    Garbalińska G
    Ann Acad Med Stetin; 1982; 28():235-48. PubMed ID: 6820238
    [No Abstract]   [Full Text] [Related]  

  • 5. [Study on application of CODIS loci to excluding paternity].
    Fang JX; Liu XJ; Cheng DL
    Fa Yi Xue Za Zhi; 2001 May; 17(2):86-8. PubMed ID: 12533863
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Excerpts from the expert opinion about the content of the publication HEIDE, PETERSEN, BRINKMANN: "Forensic value of quantitative studies of erythrocyte acid phosphatase and GPT blood components in the clarification of disputed parentage." (Published 1974 in this journal)].
    Ritter H
    Z Rechtsmed; 1975 Nov; 76(3):233-4. PubMed ID: 1217211
    [No Abstract]   [Full Text] [Related]  

  • 7. Minisequencing-based genotyping of Duffy and ABO blood groups for forensic purposes.
    Ferri G; Bini C; Ceccardi S; Ingravallo F; Lugaresi F; Pelotti S
    J Forensic Sci; 2006 Mar; 51(2):357-60. PubMed ID: 16566771
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new case of a silent allele in the PGM system.
    Herzog P; Libich M
    Hum Hered; 1982; 32(4):293-5. PubMed ID: 6215330
    [No Abstract]   [Full Text] [Related]  

  • 9. [Gc- Tf-subtypes in Vienna and their usefulness in paternity testing (author's transl)].
    Pausch V; Weirather M; Mayr WR
    Wien Klin Wochenschr; 1980 Nov; 92(21):756-9. PubMed ID: 7467353
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Exclusion of paternity with the aid of blood groups].
    Matte J
    Laval Med; 1970 Nov; 41(11):1081-4. PubMed ID: 4991444
    [No Abstract]   [Full Text] [Related]  

  • 11. [Calculation of gene-frequencies of the Ka sign and degree of exclusion probability using this sign in serological paternity expert evaluation].
    Klose I
    Beitr Gerichtl Med; 1973; 30():214-6. PubMed ID: 4540824
    [No Abstract]   [Full Text] [Related]  

  • 12. Determination of sibling relationship and paternity.
    Pérez-Comas A
    Bol Asoc Med P R; 1982 Mar; 74(3):82-7. PubMed ID: 6957200
    [No Abstract]   [Full Text] [Related]  

  • 13. Occurrence of EsD0 gene in the Polish population.
    Schlesinger D; Hałasa J
    Arch Immunol Ther Exp (Warsz); 1982; 30(1-2):115-20. PubMed ID: 7149921
    [No Abstract]   [Full Text] [Related]  

  • 14. The structure of a variant allele which is considered to be 30.3 in the STR locus D21S11.
    Tsuji A; Ishiko A; Ikeda N
    Leg Med (Tokyo); 2006 May; 8(3):182-3. PubMed ID: 16515880
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The phenomenon of gene linkage and recombination in the paternity test].
    Cheng DL; Yan PH; Liu Y; Chen J
    Fa Yi Xue Za Zhi; 1999 Feb; 15(1):31-2, 64. PubMed ID: 12536396
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel cis-AB allele derived from the A transferase gene by nucleotide substitution C796A.
    Chen DP; Tseng CP; Wang WT; Wang MC; Tsao KC; Wu TL; Sun CF
    Ann Clin Lab Sci; 2004; 34(4):437-42. PubMed ID: 15648786
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variation in recombination frequencies in Schizophyllum commune and its genetic control.
    Tang CY; Chang ST
    Aust J Biol Sci; 1974 Feb; 27(1):103-10. PubMed ID: 4596396
    [No Abstract]   [Full Text] [Related]  

  • 18. Immunogenetics of insulin-dependent juvenile diabetes.
    Dausset J; Hors J
    Diabetes Res; 1984 Sep; 1(3):115-23. PubMed ID: 6085045
    [No Abstract]   [Full Text] [Related]  

  • 19. Molecular genetics of RH and its clinical application.
    Flegel WA
    Transfus Clin Biol; 2006; 13(1-2):4-12. PubMed ID: 16563832
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Grandmother/mother/child-incompatibility due to rhesus gene complexes (C)D(e)].
    Trube-Becker E; Henke J
    Z Morphol Anthropol; 1981; 72(2):205-12. PubMed ID: 6797138
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.