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 *

107 related articles for article (PubMed ID: 1081890)

  • 1. Report of the Committee on the Genetic Constitution of the X Chromosome.
    Birth Defects Orig Artic Ser; 1975; 11(3):20-5. PubMed ID: 1081890
    [No Abstract]   [Full Text] [Related]  

  • 2. The linkage between Duchenne-type progressive muscular dystrophy and color blindness.
    Prot J; Laska M
    Pol Med J; 1970; 9(5):1207-11. PubMed ID: 5313771
    [No Abstract]   [Full Text] [Related]  

  • 3. [Human chromosome mapping].
    Frézal J; Nguyen Van Cong
    Nouv Presse Med; 1979 Mar; 8(10):769-74. PubMed ID: 313554
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetic counseling in sex linkage.
    Morton NE; Lalouel JM
    Birth Defects Orig Artic Ser; 1979; 15(5C):9-24. PubMed ID: 393324
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular genetics of the X chromosome and X-linked diseases.
    Craig IW; Goodfellow PN
    Lab Invest; 1986 Mar; 54(3):241-53. PubMed ID: 3512907
    [No Abstract]   [Full Text] [Related]  

  • 6. Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.
    Skinner R; Smith C; Emery AE
    J Med Genet; 1974 Dec; 11(4):317-20. PubMed ID: 4548442
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Report of the committee on the genetic constitution of chromosomes 10, 11, 12, X, and Y.
    de la Chapelle A; Miller OJ
    Birth Defects Orig Artic Ser; 1980; 15(11):47-58. PubMed ID: 6938255
    [No Abstract]   [Full Text] [Related]  

  • 8. New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.
    Zatz M; Itskan SB; Sanger R; Frota-Pessoa O; Saldanha PH
    J Med Genet; 1974 Dec; 11(4):321-7. PubMed ID: 4548443
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gonosomal aberrations and congenital dyschromatopsias.
    François J
    Mod Probl Ophthalmol; 1974; 13(0):231-47. PubMed ID: 4548140
    [No Abstract]   [Full Text] [Related]  

  • 10. Report of the committee on the genetic constitution of the X and Y chromosomes.
    Brown JA; Goss S; Klinger HP; Miller OJ; Ohno S; Siniscalco M
    Birth Defects Orig Artic Ser; 1976; 12(7):54-9. PubMed ID: 1024653
    [No Abstract]   [Full Text] [Related]  

  • 11. X-linked haematological traits.
    Kerr CB
    Bibl Haematol; 1968; 29():59-70. PubMed ID: 5303926
    [No Abstract]   [Full Text] [Related]  

  • 12. [Heredity of congenital deficiencies in color vision].
    François J; De Bie S; Verriest G; Matton MT
    Acta Genet Med Gemellol (Roma); 1972 Jul; 21(3):233-56. PubMed ID: 4592447
    [No Abstract]   [Full Text] [Related]  

  • 13. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy.
    Murray JM; Davies KE; Harper PS; Meredith L; Mueller CR; Williamson R
    Nature; 1982 Nov; 300(5887):69-71. PubMed ID: 6982420
    [No Abstract]   [Full Text] [Related]  

  • 14. Use of genetic linkage for the detection of female carriers of hemophilia.
    McCurdy PR
    N Engl J Med; 1971 Jul; 285(4):218-9. PubMed ID: 5087725
    [No Abstract]   [Full Text] [Related]  

  • 15. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH
    Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797
    [No Abstract]   [Full Text] [Related]  

  • 16. Gene mapping and the muscular dystrophies.
    Harper PS
    Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
    [No Abstract]   [Full Text] [Related]  

  • 17. The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.
    Emery AE; Smith CA; Sanger R
    Ann Hum Genet; 1969 Jan; 32(3):261-9. PubMed ID: 5305175
    [No Abstract]   [Full Text] [Related]  

  • 18. Lack of association between color blindness and alcoholism.
    Riffenburgh RS; Shea JF
    Eye Ear Nose Throat Mon; 1970 May; 49(5):240-2. PubMed ID: 5312326
    [No Abstract]   [Full Text] [Related]  

  • 19. Report of the committee on the genetic constitution of chromosome 6.
    Weitkamp LR; Lamm LU
    Birth Defects Orig Artic Ser; 1982; 18(2):130-43. PubMed ID: 6760916
    [No Abstract]   [Full Text] [Related]  

  • 20. Report of the committee on the genetic constitution of chromosome 6.
    Francke U; Weitkamp LR
    Birth Defects Orig Artic Ser; 1980; 15(11):32-8. PubMed ID: 6938253
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.