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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

171 related items for PubMed ID: 1867262

  • 1. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.
    Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M.
    Am J Med Genet; 1991 Apr 01; 39(1):38-41. PubMed ID: 1867262
    [Abstract] [Full Text] [Related]

  • 2. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance.
    Zatz M, Passos-Bueno MR, Rapaport D.
    Am J Med Genet; 1989 Mar 01; 32(3):407-10. PubMed ID: 2658592
    [Abstract] [Full Text] [Related]

  • 3. Familial occurrence of Duchenne dystrophy through paternal lines in four families.
    Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M.
    Am J Med Genet; 1991 Jan 01; 38(1):80-4. PubMed ID: 1849353
    [Abstract] [Full Text] [Related]

  • 4. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
    Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M.
    Am J Med Genet; 1991 Jan 01; 38(1):140-6. PubMed ID: 2012126
    [Abstract] [Full Text] [Related]

  • 5. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S, Sugino S, Ohtani Y, Matsukura M, Nishino I, Ikezawa M, Sakata A, Kondo Y, Yoshioka K, Huard J, Nonaka I, Miike T.
    Ann Neurol; 1998 Dec 01; 44(6):967-71. PubMed ID: 9851444
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 01; 32(2):268-73. PubMed ID: 2648829
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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 01; 25(2):211-8. PubMed ID: 3777018
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
    Wilton SD, Chandler DC, Kakulas BA, Laing NG.
    Hum Mutat; 1994 Oct 01; 3(2):133-40. PubMed ID: 8199594
    [Abstract] [Full Text] [Related]

  • 18. Duchenne muscular dystrophy.
    Matsuo M.
    Southeast Asian J Trop Med Public Health; 1995 Oct 01; 26 Suppl 1():166-71. PubMed ID: 8629099
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.