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 *

104 related articles for article (PubMed ID: 2759620)

  • 1. Genetic genealogical studies of 20 north Swedish families with the rare blood group p.
    Nordström S; Cedergren B
    Hum Hered; 1989; 39(1):20-5. PubMed ID: 2759620
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th century.
    Holmgren G; Blomquist HK; Drugge U; Gustavson KH
    Am J Med Genet; 1988; 30(1-2):673-9. PubMed ID: 3052071
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLO-SL): a genealogical study of Swedish families of probable Finnish background.
    Nylander PO; Drugge U; Holmgren G; Adolfsson R
    Clin Genet; 1996 Nov; 50(5):353-7. PubMed ID: 9007323
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth century.
    Drugge U; Blomquist HK; Gustavson KH; Holmgren G
    Am J Med Genet; 1991; 38(2-3):363-6. PubMed ID: 2018076
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variable expression of tapetoretinal degeneration in northern Sweden.
    Nordström S
    Hereditas; 1993; 118(1):15-9. PubMed ID: 8478206
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.
    Fuchs J; Nilsson C; Kachergus J; Munz M; Larsson EM; Schüle B; Langston JW; Middleton FA; Ross OA; Hulihan M; Gasser T; Farrer MJ
    Neurology; 2007 Mar; 68(12):916-22. PubMed ID: 17251522
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duffy, Kell and P blood group systems in some Jewish populations of Israel.
    Kobyliansky E; Micle S; Goldschmidt-Nathan M; Arensburg B; Nathan H
    Acta Anthropogenet; 1980; 4(3-4):173-9. PubMed ID: 7346047
    [TBL] [Abstract][Full Text] [Related]  

  • 8. p Phenotype in an Ecuadorian family.
    Sweeney JD; Wenz B
    Transfusion; 1984; 24(1):25-7. PubMed ID: 6695437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Personalized genealogical history of UK individuals inferred from biobank-scale IBD segments.
    Naseri A; Tang K; Geng X; Shi J; Zhang J; Shakya P; Liu X; Zhang S; Zhi D
    BMC Biol; 2021 Feb; 19(1):32. PubMed ID: 33593342
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hemolyzing antibodies to markers of the P blood factor system as a problem in blood transfusion and pregnancy. With reference to serology, biochemistry and genetics].
    Pausch V; Speiser P; Michl U; Höcker P; Engelfriet CP
    Wien Klin Wochenschr; 1990 Feb; 102(3):80-90. PubMed ID: 2316222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is there a positive assortative mating for the P blood group?
    Rasmuson M; Valentin J
    Hum Hered; 1983; 33(1):9-12. PubMed ID: 6840785
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Population studies in northern Sweden. XI. The Duffy blood group polymorphism.
    Cedergren B; Nordenson I; Beckman L
    Hum Hered; 1983; 33(6):365-70. PubMed ID: 6674112
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic aspects of genealogy].
    Tetushkin EIu
    Genetika; 2011 Nov; 47(11):1451-72. PubMed ID: 22332404
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Vel blood group in northern Sweden.
    Cedergren B; Giles CM; Ikin EW
    Vox Sang; 1976 Nov; 31(5):344-55. PubMed ID: 1007157
    [TBL] [Abstract][Full Text] [Related]  

  • 15. P phenotype observed in two generations of Tunisian family with a high rate of inbreeding.
    Salmon D; Bouchmel S; Hafsia A; Boussen S; Boussen M; Bouguerra A
    Rev Fr Transfus Immunohematol; 1979 Dec; 22(5):563-71. PubMed ID: 547353
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22.
    Eiberg H; Møller N; Mohr J; Nielsen LS
    Clin Genet; 1986 May; 29(5):354-9. PubMed ID: 3461892
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A Swiss family with the red cell antigen Pk (author's transl)].
    Gerber H; Labhard S; Bütler R; Hässig A
    Wien Klin Wochenschr; 1980 Nov; 92(21):752-4. PubMed ID: 7467352
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gaucher disease (Norrbottnian type III): probable founders identified by genealogical and molecular studies.
    Dahl N; Hillborg PO; Olofsson A
    Hum Genet; 1993 Nov; 92(5):513-5. PubMed ID: 8244344
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genealogic methods].
    Czeizel E
    Orv Hetil; 1989 May; 130(20):1061-3. PubMed ID: 2660060
    [No Abstract]   [Full Text] [Related]  

  • 20. Polymorphism of ABO, MN, rhesus and P blood groups among four east Georgian populations.
    Nasidze IS
    Gene Geogr; 1992; 6(1-2):85-8. PubMed ID: 1299318
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.