BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 4435793)

  • 1. Assignment of the major histocompatibility complex to chromosome No. 6 in a family with a pericentric inversion.
    Lamm LU; Friedrich U; Petersen CB; Jorgensen J; Nielsen J; Therkelsen AJ; Kissmeyer-Nielsen F
    Hum Hered; 1974; 24(3):273-84. PubMed ID: 4435793
    [No Abstract]   [Full Text] [Related]  

  • 2. Pericentric inversions of human chromosomes 9 and 10.
    de la Chapelle A; Schröder J; Stenstrand K; Fellman J; Herva R; Saarni M; Anttolainen I; Tallila I; Tervilä L; Husa L; Tallqvist G; Robson EB; Cook PJ; Sanger R
    Am J Hum Genet; 1974 Nov; 26(6):746-66. PubMed ID: 4140690
    [No Abstract]   [Full Text] [Related]  

  • 3. Pericentric inversion of a group C autosome: a study of three families.
    Jacobs PA; Cruickshank G; Faed MJ; Frackiewicz A; Robson EB; Harris H; Sutherland I
    Ann Hum Genet; 1968 Jan; 31(3):219-30. PubMed ID: 5648745
    [No Abstract]   [Full Text] [Related]  

  • 4. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 5. Inherited pericentric inversion of a group D (13-15) chromosome.
    Surana RB; Conen PE
    J Med Genet; 1972 Mar; 9(1):105-10. PubMed ID: 5025473
    [No Abstract]   [Full Text] [Related]  

  • 6. A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.
    Soukup SW; Yarema W; Robinow M
    Humangenetik; 1974; 25(1):69-78. PubMed ID: 4442881
    [No Abstract]   [Full Text] [Related]  

  • 7. Possible linear order of genes for endocrine neoplasia type 2, the P red cell antigen and HL-A on chromosome 6.
    Jackson CE; Conneally PM; Sizemore GW; Tashjian AH
    Birth Defects Orig Artic Ser; 1976; 12(1):159-64. PubMed ID: 990440
    [No Abstract]   [Full Text] [Related]  

  • 8. Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA).
    Merritt AD; Petersen BH; Biegel AA; Meyers DA; Brooks GF; Hodes ME
    Cytogenet Cell Genet; 1976; 16(1-5):331-4. PubMed ID: 975903
    [No Abstract]   [Full Text] [Related]  

  • 9. A genetic linkage analysis of chromosome 6 markers Chido, HLA, and glyoxalase.
    Lewis M; Kaita H; Chown B; Bowen P; Lee CS; McDonald S; Giblett ER; Anderson J; Dossetor JB; Schlaut J; Pai KR; Singal DP; Steinberg AG
    Cytogenet Cell Genet; 1976; 16(1-5):317-21. PubMed ID: 975899
    [No Abstract]   [Full Text] [Related]  

  • 10. Autosomal linkage in humans (methodology and results of computer analysis).
    Falk CT; Walker ME; Martin MD; Allen FH
    Ser Haematol; 1975; 8(2):153-237. PubMed ID: 1198129
    [No Abstract]   [Full Text] [Related]  

  • 11. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.
    Jackson JF; Currier RD; Terasaki PI; Morton NE
    N Engl J Med; 1977 May; 296(20):1138-41. PubMed ID: 857157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Histocompatibility in the rabbit. Linkage between RL-A, MLC, and the He blood group loci.
    Tissot RG; Cohen C
    Transplantation; 1974 Aug; 18(2):142-9. PubMed ID: 4276720
    [No Abstract]   [Full Text] [Related]  

  • 13. Pericentric Y inversion in the general population.
    Zeuthen E; Nielsen J
    Humangenetik; 1973 Sep; 19(3):265-70. PubMed ID: 4763930
    [No Abstract]   [Full Text] [Related]  

  • 14. C3 polymorphism: genetic linkage relations.
    Gedde-Dahl T; Teisberg P; Thorsby E
    Clin Genet; 1974; 6(1):66-72. PubMed ID: 4426132
    [No Abstract]   [Full Text] [Related]  

  • 15. Inversion homozygosity of chromosome no. 9 in a higly inbred kindred.
    Vine DT; Yarkoni S; Cohen MM
    Am J Hum Genet; 1976 May; 28(3):203-7. PubMed ID: 233959
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The HL-A system. I. Genetics and molecular biology.
    Ceppellini R; van Rood JJ
    Semin Hematol; 1974 Jul; 11(3):233-51. PubMed ID: 4151844
    [No Abstract]   [Full Text] [Related]  

  • 17. Blood groups in human genetics.
    Race RR
    Bibl Haematol; 1971; 37():10-20. PubMed ID: 5167756
    [No Abstract]   [Full Text] [Related]  

  • 18. Giemsa banding of chromosome 1gh+ and linkage analysis.
    Howard PN; Stoddard GR; Goddard MW; Seely JR
    J Med Genet; 1975 Mar; 12(1):44-8. PubMed ID: 47395
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.
    Kimberling WJ; Fulbeck T; Dixon L; Lubs HA
    Am J Hum Genet; 1975 Sep; 27(5):586-94. PubMed ID: 1163534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic and linkage studies of a familial 15pplus variant.
    Yoder FE; Bias WB; Borgaonkar DS; Bahr GF; Yoder II; Yoder OC; Golomb HM
    Am J Hum Genet; 1974 Sep; 26(5):535-48. PubMed ID: 4138462
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.