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

Journal Abstract Search


130 related items for PubMed ID: 3806639

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias].
    Rotthauwe HW, Mortier W, Beyer H.
    Humangenetik; 1972; 16(3):181-200. PubMed ID: 5082100
    [No Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Emery-Dreifuss syndrome and X-linked muscular dystrophy with contractures: evidence for homogeneity.
    Goldblatt J, Schram LJ, Wallis G, Oswald A, Beighton P.
    Clin Genet; 1989 Jan; 35(1):1-4. PubMed ID: 2924429
    [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. [A family of scapula-back type of x-linked recessive muscular dystrophy].
    Ji XW.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):136-8, 190. PubMed ID: 2591265
    [Abstract] [Full Text] [Related]

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

  • 11. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.
    Bol Med Hosp Infant Mex; 1981 Jun; 38(1):23-33. PubMed ID: 7284070
    [Abstract] [Full Text] [Related]

  • 12. Emery-Dreifuss syndrome.
    Tsuchiya Y, Arahata K.
    Curr Opin Neurol; 1997 Oct; 10(5):421-5. PubMed ID: 9330889
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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 11; 66(2):237-8. PubMed ID: 8958338
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Benign muscular dystrophy with contractures: a new syndrome?
    Bailey RO, Dentinger MP, Toms ME, Hans MB.
    Acta Neurol Scand; 1986 Apr 11; 73(4):439-43. PubMed ID: 3727920
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Reflections on muscular dystrophy in a Sudanese kindred.
    Salih MA, Roberts DF, Omer MI, Karrar O, Bayoumi RA.
    Clin Genet; 1983 Apr 11; 23(4):325-8. PubMed ID: 6851225
    [Abstract] [Full Text] [Related]

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

  • 20. Spinal muscular atrophy and probable Duchenne muscular dystrophy occurring separately in closely related Melanesian families in Papua, New Guinea.
    Scrimgeour EM, Mastaglia FL, Kevau I.
    Am J Med Genet; 1992 Aug 01; 43(6):1044-5. PubMed ID: 1415334
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.