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 *

183 related articles for article (PubMed ID: 5149523)

  • 41. [Ocular findings in patients with Steinert myotonic dystrophy].
    Markowska E; Zalewska R; Mariak Z; Wojnar M
    Przegl Lek; 2006; 63(8):662-3. PubMed ID: 17441379
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Failure to demonstrate linkage between the loci for the Rh and Duffy blood groups.
    Sanger R; Tippett P; Gavin J; Race RR
    Ann Hum Genet; 1973 Jan; 36(3):353-4. PubMed ID: 4714425
    [No Abstract]   [Full Text] [Related]  

  • 44. Minimal expression of myotonic dystrophy: a clinical and molecular analysis.
    Reardon W; Harley HG; Brook JD; Rundle SA; Crow S; Harper PS; Shaw DJ
    J Med Genet; 1992 Nov; 29(11):770-3. PubMed ID: 1453424
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
    Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT
    JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Myotonia dystrophica].
    Grinshteĭn AB; Goretov AP; Belyĭ EA
    Zh Nevrol Psikhiatr Im S S Korsakova; 1993; 93(5):17-9. PubMed ID: 8154209
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.
    Mahadevan MS; Foitzik MA; Surh LC; Korneluk RG
    Genomics; 1993 Feb; 15(2):446-8. PubMed ID: 8449517
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
    Eiberg H; Mohr J; Nielsen LS; Simonsen N
    Clin Genet; 1983 Sep; 24(3):159-70. PubMed ID: 6627719
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Myotonic muscular dystrophy--molecular genetics 1994].
    Achiron A; Hamiel-Pinhas O; Gadoth N
    Harefuah; 1994 Jun; 126(11):664-7. PubMed ID: 7927002
    [No Abstract]   [Full Text] [Related]  

  • 50. Meiotic drive at the myotonic dystrophy locus?
    Carey N; Johnson K; Nokelainen P; Peltonen L; Savontaus ML; Juvonen V; Anvret M; Grandell U; Chotai K; Robertson E
    Nat Genet; 1994 Feb; 6(2):117-8. PubMed ID: 8162064
    [No Abstract]   [Full Text] [Related]  

  • 51. Advances in myotonic dystrophy: a clinical and genetic perspective.
    Reardon W; Harper PS
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):605-9. PubMed ID: 1392133
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Manic-depressive illness: linkage with the Xg blood group.
    Fieve RR; Mendlewicz J; Fleiss JL
    Am J Psychiatry; 1973 Dec; 130(12):1355-9. PubMed ID: 4754680
    [No Abstract]   [Full Text] [Related]  

  • 53. Linkage relations among 25 autosomal blood, urine, and saliva markers in two large multigenerational pedigrees.
    Namboodiri KK; Elston RC; Go RC
    Cytogenet Cell Genet; 1978; 22(1-6):633-9. PubMed ID: 752558
    [No Abstract]   [Full Text] [Related]  

  • 54. Evolutionary significance of the HL-A system.
    Bodmer WF
    Nature; 1972 May; 237(5351):139-45 passim. PubMed ID: 4113158
    [No Abstract]   [Full Text] [Related]  

  • 55. [A case of myotonic dystrophy proved by DNA analysis].
    Juryńczyk J; Weglewski A
    Neurol Neurochir Pol; 1998; 32(5):1267-71. PubMed ID: 10463239
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Introduction to blood group genetics.
    Polesky HF
    Mayo Clin Proc; 1977 Mar; 52(3):136-40. PubMed ID: 402510
    [No Abstract]   [Full Text] [Related]  

  • 57. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
    Meredith AL; Huson SM; Lunt PW; Sarfarazi M; Harley HG; Brook JD; Shaw DJ; Harper PS
    Br Med J (Clin Res Ed); 1986 Nov; 293(6558):1353-6. PubMed ID: 2878705
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W; Floyd JL; Myring J; Lazarou LP; Meredith AL; Harper PS
    Am J Med Genet; 1992 Aug; 43(6):1006-11. PubMed ID: 1415325
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.
    Ott J
    Am J Hum Genet; 1974 Sep; 26(5):588-97. PubMed ID: 4422075
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.