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 *

684 related articles for article (PubMed ID: 6585139)

  • 1. Easy calculations of lod scores and genetic risks on small computers.
    Lathrop GM; Lalouel JM
    Am J Hum Genet; 1984 Mar; 36(2):460-5. PubMed ID: 6585139
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.
    Andrews DF; Brasher PM; Manchester KE; Percy ME; Rusk AC; Soltan HC; Trueman DW
    Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.
    Baranzini SE; Giliberto F; Dalamon V; Barreiro C; García-Erro M; Grippo J; Szijan I
    Clin Genet; 1998 Dec; 54(6):503-11. PubMed ID: 9894797
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy.
    Emery AE; Holloway S
    Hum Hered; 1977; 27(2):118-26. PubMed ID: 863458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
    Lindlöf M; Sistonen P; de la Chapelle A
    Ann Hum Genet; 1987 Oct; 51(4):317-28. PubMed ID: 3482147
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

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

  • 11. A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophy.
    Jardine PE; Upadhyaya M; Maynard J; Harper P; Lunt PW
    Neuromuscul Disord; 1994; 4(5-6):477-82. PubMed ID: 7881292
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.
    Brown CS; Thomas NS; Sarfarazi M; Davies KE; Kunkel L; Pearson PL; Kingston HM; Shaw DJ; Harper PS
    Hum Genet; 1985; 71(1):62-74. PubMed ID: 2993158
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes.
    Clayton J
    Hum Genet; 1986 May; 73(1):68-72. PubMed ID: 3458666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Reflections on muscular dystrophy in a Sudanese kindred.
    Salih MA; Roberts DF; Omer MI; Karrar O; Bayoumi RA
    Clin Genet; 1983 Apr; 23(4):325-8. PubMed ID: 6851225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C).
    Ben Othmane K; Speer MC; Stauffer J; Blel S; Middleton L; Ben Hamida C; Etribi A; Loeb D; Hentati F; Roses AD
    Am J Hum Genet; 1995 Sep; 57(3):732-4. PubMed ID: 7668303
    [No Abstract]   [Full Text] [Related]  

  • 17. The use of serum creatine phosphokinase in genetic counseling for Duchenne muscular dystrophy. I. Analysis of results from 29 studies.
    Gale AN; Murphy EA
    J Chronic Dis; 1978 Feb; 31(2):101-9. PubMed ID: 659567
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic counseling in Becker type X-linked muscular dystrophy. II: Practical considerations.
    Grimm T
    Am J Med Genet; 1984 Aug; 18(4):719-23. PubMed ID: 6486170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A linkage study of Emery-Dreifuss muscular dystrophy.
    Hodgson S; Boswinkel E; Cole C; Walker A; Dubowitz V; Granata C; Merlini L; Bobrow M
    Hum Genet; 1986 Dec; 74(4):409-16. PubMed ID: 3466853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetics of muscular dystrophies].
    Harper PS
    Recenti Prog Med; 1977 May; 62(5):489-511. PubMed ID: 329369
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 35.