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 *

116 related articles for article (PubMed ID: 955636)

  • 1. Human red cell acid phosphatase: quantitative evidence of a silent gene PO, and a Danish population study.
    Dissing J; Svensmark O
    Hum Hered; 1976; 26(1):43-58. PubMed ID: 955636
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Quantitative evidence of a silent gene Po of human red cell acid phosphatase in south Polish population.
    Turowska B; Bogusz M; Stojek T
    Forensic Sci; 1977; 10(2):109-16. PubMed ID: 903046
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human red cell galactose-1-phosphate uridylyltransferase (EC 2.7.7.12). Electrophoretically determined polymorphism in Denmark and its use in paternity cases.
    Eriksen B; Dissing J
    Hum Hered; 1980; 30(1):27-32. PubMed ID: 6243609
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human red cell esterase D polymorphism in Denmark, its use in paternity cases and the description of a new phenotype.
    Dissing J; Eriksen B
    Hum Hered; 1984; 34(3):148-55. PubMed ID: 6469261
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human red cell acid phosphatase polymorphism. A study on gene frequency and forensic use of the system in cases of disputed paternity.
    Fuhrmann W; Lichte KH
    Humangenetik; 1966; 3(2):121-6. PubMed ID: 5984973
    [No Abstract]   [Full Text] [Related]  

  • 6. The red cell acid phosphatase polymorphism in Sweden. Gene frequencies and application to disputed paternity.
    Broman P; Grundin R; Lins PE
    Acta Genet Med Gemellol (Roma); 1971 Jan; 20(1):77-81. PubMed ID: 5568113
    [No Abstract]   [Full Text] [Related]  

  • 7. Human red cell glyoxalase I polymorphism in Denmark and its application to paternity cases.
    Eriksen B
    Hum Hered; 1979; 29(5):265-71. PubMed ID: 489026
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human red cell acid phosphatase polymorphism. Population and family studies in Denmark.
    Sorensen SA
    Hum Hered; 1973; 23(5):470-81. PubMed ID: 4785875
    [No Abstract]   [Full Text] [Related]  

  • 9. [The study of acid phosphatase content in erythrocytes in disputed paternity cases].
    Szabó L; Haán A; Péchy O; Somogyi E
    Morphol Igazsagugyi Orv Sz; 1975 Apr; 15(2):113-9. PubMed ID: 1128532
    [No Abstract]   [Full Text] [Related]  

  • 10. Family studies of red cell acid phosphatase types. Report of a family with the D variant.
    Lamm LU
    Hum Hered; 1970; 20(3):329-35. PubMed ID: 5489889
    [No Abstract]   [Full Text] [Related]  

  • 11. Evidence of a "new" allele of red cell and phosphatase AcPk.
    Turowska B
    Forensic Sci Int; 1984 Nov; 26(3):163-7. PubMed ID: 6595186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A silent allele for red cell acid phosphatase in a Polish family.
    Raczek E; Grzesik J
    Hum Hered; 1986; 36(5):339-40. PubMed ID: 3759110
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The utility of red cell acid phosphatase in paternity testing.
    Wyslouchowa B
    Acta Med Pol; 1969; 10(1):69-74. PubMed ID: 5784096
    [No Abstract]   [Full Text] [Related]  

  • 14. Atypical segregation of human red cell acid phosphatase phenotypes: evidence for a rare 'silent' allele Po.
    Herbich J; Fisher RA; Hopkinson DA
    Ann Hum Genet; 1970 Oct; 34(2):145-51. PubMed ID: 5493843
    [No Abstract]   [Full Text] [Related]  

  • 15. The rare silent gene Po of human red cell acid phosphatase in a second family in Poland.
    Turowska B; Bogusz M
    Forensic Sci; 1978; 11(3):175-6. PubMed ID: 680608
    [No Abstract]   [Full Text] [Related]  

  • 16. Polymorphism of the red cell acid phosphatase in the Swiss population.
    Pflugshaupt R; Scherz R; Trautwein M; Richiger U; Bütler R
    Humangenetik; 1970; 8(4):354-6. PubMed ID: 5436704
    [No Abstract]   [Full Text] [Related]  

  • 17. A case study of paternity diagnosis where phenotypes CA and CB of erythrocyte acid phosphatase were found in a putative father and a child, respectively.
    Minakata K; Asano M
    Nihon Hoigaku Zasshi; 1986 Apr; 40(2):146-9. PubMed ID: 3784116
    [No Abstract]   [Full Text] [Related]  

  • 18. [Forensic importance of spectrophotometric tests of the isoenzyme systems red cell acid phosphatase and glutamatic-pyruvic transaminase in settlement of paternity disputes (author's transl)].
    Heide KG; Petersen N; Brinkmann B
    Z Rechtsmed; 1974 Jun; 74(3):177-80. PubMed ID: 4848789
    [No Abstract]   [Full Text] [Related]  

  • 19. [Exclusions of paternity by means of erythrocyte phosphatase].
    Prokop O; Radam G; Strauch H
    Z Arztl Fortbild (Jena); 1966 Jun; 60(11):691-2. PubMed ID: 5994877
    [No Abstract]   [Full Text] [Related]  

  • 20. Polymorphism of the human phosphoglycolate phosphatase in Northrhine-Westphalia (F.R.G.) and its application to paternity testing.
    Henke J; Basler M; Baur MP
    Forensic Sci Int; 1983; 22(2-3):137-42. PubMed ID: 6315552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.