BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 896656)

  • 1. [Carrier detection and genetic counselling in duchenne muscular dystrophy (author's transl)].
    Moser H
    Schweiz Rundsch Med Prax; 1977 Jul; 66(27):814-22. PubMed ID: 896656
    [No Abstract]   [Full Text] [Related]  

  • 2. DNA analysis and genetic counselling in Duchenne muscular dystrophy.
    Gardner RJ; Wilson SJ; Wilkins RJ
    N Z Med J; 1988 Jul; 101(849):455-7. PubMed ID: 3399183
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effects of genetic counseling on Duchenne muscular dystrophy families in Brazil.
    Zatz M
    Am J Med Genet; 1983 Jul; 15(3):483-90. PubMed ID: 6881214
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Genetic counselling for Duchenne muscular dystrophy].
    Ousawa M; Saito K; Ikeya K; Fukuyama Y
    No To Shinkei; 1991 May; 43(5):429-41. PubMed ID: 1910929
    [No Abstract]   [Full Text] [Related]  

  • 5. Carrier detection and genetic counselling in Duchenne muscular dystrophy: a follow-up study.
    Hutton EM; Thompson MW
    Can Med Assoc J; 1976 Oct; 115(8):749-52. PubMed ID: 974964
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling.
    Bushby K; Goodship J; Haggerty D; Heald A; Walls T
    Am J Med Genet; 1996 Dec; 66(2):237-8. PubMed ID: 8958338
    [No Abstract]   [Full Text] [Related]  

  • 7. Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophy.
    Zellweger H; Ionasescu V; Simpson J
    Helv Paediatr Acta; 1980 Sep; 35(4):343-8. PubMed ID: 7451237
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic counseling in Duchenne muscular dystrophy.
    Dennis MR; Bundey S
    Muscle Nerve; 1981; 4(1):81-2. PubMed ID: 7231452
    [No Abstract]   [Full Text] [Related]  

  • 9. [Newborn screening for Duchenne muscular dystrophy (author's transl)].
    Grimm T
    Monatsschr Kinderheilkd; 1981 Jul; 129(7):414-7. PubMed ID: 6115310
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW; Papp AC; Snyder PJ; Mendell JR
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis.
    Bakker E; Bonten EJ; den Dunnen JT; Veenema H; Grootscholten PM; van Ommen GJ; Pearson PL
    Prog Clin Biol Res; 1989; 306():51-67. PubMed ID: 2662213
    [No Abstract]   [Full Text] [Related]  

  • 13. Potential pitfalls in using DNA probes to counsel Duchenne and Becker muscular dystrophy families.
    Shi YJ; Fischbeck KH; Ritter A
    Chin Med J (Engl); 1992 Jun; 105(6):469-75. PubMed ID: 1451547
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic counseling in Duchenne muscular dystrophy].
    Martínez Matos JA
    Neurologia; 1989 Oct; 4(8):265-7. PubMed ID: 2637768
    [No Abstract]   [Full Text] [Related]  

  • 15. Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels.
    Muir WA; Knoke J; Martin A; Vignos P; McErlean A
    Am J Med Genet; 1983 Jan; 14(1):125-34. PubMed ID: 6829600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic counseling issues in the use of DNA analysis for Duchenne/Becker muscular dystrophy.
    Cortada JM; Milsark I; Richards CS
    Birth Defects Orig Artic Ser; 1990; 26(3):231-7. PubMed ID: 2092850
    [No Abstract]   [Full Text] [Related]  

  • 17. Duchenne muscular dystrophy: a genetic approach for disease prevention.
    Cohan L; Caskey CT
    Tex Med; 1981 May; 77(5):58-60. PubMed ID: 7233341
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P
    Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pyruvate-kinase (PK) and creatine-kinase (CK) in normal pregnancy and its implication in genetic counseling of Duchenne muscular dystrophy (DMD).
    Zatz M; Karp LE; Rogatko A
    Am J Med Genet; 1982 Nov; 13(3):257-62. PubMed ID: 7180871
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Screening for Duchenne muscular dystrophy].
    Beckmann R
    Offentl Gesundheitswes; 1981 Sep; 43(9):414-20. PubMed ID: 6213887
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.