BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 7390481)

  • 1. Duchenne muscular dystrophy: data from family studies.
    Danieli GA; Mostacciuolo ML; Pilotto G; Angelini C; Bonfante A
    Hum Genet; 1980; 54(1):63-8. PubMed ID: 7390481
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duchenne muscular dystrophy. Frequency of sporadic cases.
    Danieli GA; Barbujani G
    Hum Genet; 1984; 67(3):252-6. PubMed ID: 6469240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epidemiology of Duchenne muscular dystrophy in the province of Turin.
    Bertolotto A; De Marchi M; Doriguzzi C; Mongini T; Monnier C; Palmucci L; Schiffer D; Verzé L
    Ital J Neurol Sci; 1981 Jan; 2(1):81-4. PubMed ID: 6977513
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Population data on benign and severe forms of X-linked muscular dystrophy.
    Mostacciuolo ML; Lombardi A; Cambissa V; Danieli GA; Angelini C
    Hum Genet; 1987 Mar; 75(3):217-20. PubMed ID: 3557448
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pedigree testing in Duchenne muscular dystrophy.
    Roses AD; Roses MJ; Metcalf BS; Hull KL; Nicholson GA; Hartwig GB; Roe CR
    Ann Neurol; 1977 Oct; 2(4):271-8. PubMed ID: 617266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A two-locus selection hypothesis for Duchenne muscular dystrophy.
    Skolnick M; Carmelli D
    Theor Popul Biol; 1977 Oct; 12(2):230-45. PubMed ID: 929458
    [No Abstract]   [Full Text] [Related]  

  • 7. Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation.
    Caskey CT; Nussbaum RL; Cohan LC; Pollack L
    Clin Genet; 1980 Nov; 18(5):329-41. PubMed ID: 7460369
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.
    Lane RJ; Robinow M; Roses AD
    J Med Genet; 1983 Feb; 20(1):1-11. PubMed ID: 6842530
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic epidemiology of Duchenne muscular dystrophy in Japan: classical segregation analysis.
    Kanamori M; Morton NE; Fujiki K; Kondo K
    Genet Epidemiol; 1987; 4(6):425-32. PubMed ID: 3428571
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophy.
    Roses AD; Roses MJ; Nicholson GA; Roe CR
    Neurology; 1977 May; 27(5):414-21. PubMed ID: 558544
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Segregation and sporadic cases of Duchenne muscular dystrophy in the Henan Province, China.
    Fu WM; Barbujani G
    Hum Hered; 1990; 40(3):167-72. PubMed ID: 2365377
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy.
    Williams WR; Thompson MW; Morton NE
    Am J Med Genet; 1983 Feb; 14(2):315-33. PubMed ID: 6837627
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibships.
    Russo A; Barbujani G; Mostacciuolo ML; Herrmann FH; Spiegler AW; Galluzzi G; Danieli GA
    Hum Genet; 1987 Jul; 76(3):230-5. PubMed ID: 3596597
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families.
    Müller CR; Grimm T
    Hum Genet; 1986 Oct; 74(2):181-3. PubMed ID: 3464560
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.
    Kaladhar Reddy B; Anandavalli TE; Reddi OS
    Hum Genet; 1984; 67(4):460-2. PubMed ID: 6490012
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.
    Davie AM; Emery AE
    J Med Genet; 1978 Oct; 15(5):339-45. PubMed ID: 739522
    [TBL] [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. Duchenne muscular dystrophy. A population study.
    Danieli GA; Mostacciuolo ML; Bonfante A; Angelini C
    Hum Genet; 1977 Feb; 35(2):225-31. PubMed ID: 844870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
    Lupski JR; Garcia CA; Zoghbi HY; Hoffman EP; Fenwick RG
    Am J Med Genet; 1991 Sep; 40(3):354-64. PubMed ID: 1683155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.