BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 5305175)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating.
    Greig DN
    J Med Genet; 1977 Apr; 14(2):130-2. PubMed ID: 300790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.
    Skinner R; Emery AE; Anderson AJ; Foxall C
    J Med Genet; 1975 Jun; 12(2):131-4. PubMed ID: 1142377
    [No Abstract]   [Full Text] [Related]  

  • 6. Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.
    Emery AE
    J Med Genet; 1966 Jun; 3(2):92-5. PubMed ID: 5297734
    [No Abstract]   [Full Text] [Related]  

  • 7. X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred.
    Went LN; De Groot WP; Sanger R; Tippett P; Gavin J
    Ann Hum Genet; 1969 May; 32(4):333-45. PubMed ID: 5307231
    [No Abstract]   [Full Text] [Related]  

  • 8. Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis.
    Adam A; Ziprkowski L; Feinstein A; Sanger R; Tippett P; Gavin J; Race RR
    Ann Hum Genet; 1969 May; 32(4):323-32. PubMed ID: 5307230
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.
    Kingston HM; Sarfarazi M; Thomas NS; Harper PS
    Hum Genet; 1984; 67(1):6-17. PubMed ID: 6086495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].
    Rotthauwe HW; Kowalewski S
    Humangenetik; 1966; 3(1):17-29. PubMed ID: 5986051
    [No Abstract]   [Full Text] [Related]  

  • 12. [An unusual form of benign hereditary recessive x-chromosomal muscular dystrophy].
    Rotthauwe HW; Beyer H
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):410. PubMed ID: 5523692
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.
    Sarfarazi M; Harper PS; Kingston HM; Murray JM; O'Brien T; Davies KE; Williamson R; Tippett P; Sanger R
    Hum Genet; 1983; 65(2):169-71. PubMed ID: 6317539
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical studies in benign (Becker type) X-linked muscular dystrophy.
    Emery AE; Skinner R
    Clin Genet; 1976 Oct; 10(4):189-201. PubMed ID: 975594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The neurogenic and myogenic hypotheses in human (Duchenne) muscular dystrophy.
    Thomson WH; Sweetin JC; Elton RA
    Nature; 1974 May; 249(453):151-2. PubMed ID: 4833513
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Duchenne's muscular dystrophy: the electrocardiogram in female relatives.
    Mann O; DeLeon AC; Perloff JK; Simanis J; Horrigan FD
    Am J Med Sci; 1968 Jun; 255():376-81. PubMed ID: 5654956
    [No Abstract]   [Full Text] [Related]  

  • 18. The manifesting carrier in Duchenne muscular dystrophy.
    Moser H; Emery AE
    Clin Genet; 1974; 5(4):271-84. PubMed ID: 4854942
    [No Abstract]   [Full Text] [Related]  

  • 19. Quantitative measurements in female siblings and mothers of boys with Duchenne dystrophy.
    Fowler WM; Gardner GW; Taylor RG; Scavarda A; Busheikin JB
    Arch Phys Med Rehabil; 1969 Jun; 50(6):301-10. PubMed ID: 5788486
    [No Abstract]   [Full Text] [Related]  

  • 20. Sex linked muscular dystrophies: severe and benign variety.
    Desai AD; Deshpande DH; Banerji AP; Jayam AV; Raju TN
    Neurol India; 1972 Dec; 20(4):163-89. PubMed ID: 4662748
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.