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Journal Abstract Search

157 related items for PubMed ID: 13637556

  • 1. Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.
    BLYTH H, PUGH RJ.
    Ann Hum Genet; 1959 Apr; 23(2):127-63. PubMed ID: 13637556
    [No Abstract] [Full Text] [Related]

  • 2. The inheritance of muscular dystrophy.
    WALTON JN.
    Acta Genet Stat Med; 1957 Apr; 7(2):318-20. PubMed ID: 13469173
    [No Abstract] [Full Text] [Related]

  • 3. Autosomal recessive inheritance of Duchennetype muscular dystrophy.
    KLOEPFER HW, TALLEY C.
    Ann Hum Genet; 1958 Feb; 22(2):138-43. PubMed ID: 13509526
    [No Abstract] [Full Text] [Related]

  • 4. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.
    KUGELBERG E, WELANDER L.
    AMA Arch Neurol Psychiatry; 1956 May; 75(5):500-9. PubMed ID: 13312732
    [No Abstract] [Full Text] [Related]

  • 5. Muscular dystrophy in Northern Ireland. III. Linkage data with particular reference to autosomal limb girdle muscular dystrophy.
    STEVENSON AC, CHEESEMAN EA.
    Ann Hum Genet; 1955 Feb; 19(3):165-73. PubMed ID: 14350450
    [No Abstract] [Full Text] [Related]

  • 6. The inheritance of neuromuscular disease.
    TYLER FH.
    Res Publ Assoc Res Nerv Ment Dis; 1954 Feb; 33():283-92. PubMed ID: 13246083
    [No Abstract] [Full Text] [Related]

  • 7. [Contribution to the study of heredity in progressive muscular dystrophy].
    PESCETTO G, FABIANI D.
    Sist Nerv; 1959 Feb; 11():383-9. PubMed ID: 14432114
    [No Abstract] [Full Text] [Related]

  • 8. Benign progressive muscular dystrophy; description of a curious family.
    KRAFT TB.
    Folia Psychiatr Neurol Neurochir Neerl; 1955 Jun; 58(3):175-86. PubMed ID: 13262229
    [No Abstract] [Full Text] [Related]

  • 9. [Progressive muscular dystrophy].
    SCHADE H.
    Munch Med Wochenschr; 1958 Apr 11; 100(15):595-7. PubMed ID: 13552675
    [No Abstract] [Full Text] [Related]

  • 10. [Progressive muscular dystrophy].
    FRIEDERICHS HF, KIRNBERGER EJ.
    Munch Med Wochenschr; 1958 Sep 19; 100(38):1444-6. PubMed ID: 13590029
    [No Abstract] [Full Text] [Related]

  • 11. [Estimation of mutation rate in muscular dystrophy].
    BECKER PE, LENZ F.
    Z Mensch Vererb Konstitutionsl; 1955 Sep 19; 33(1):42-56. PubMed ID: 13248061
    [No Abstract] [Full Text] [Related]

  • 12. Muscular dystrophy in Northern Ireland. II. An account of nine additional families.
    STEVENSON AC.
    Ann Hum Genet; 1955 Feb 19; 19(3):159-64. PubMed ID: 14350449
    [No Abstract] [Full Text] [Related]

  • 13. [A new x-chromosomal muscular dystrophy].
    BECKER PE, KIENER F.
    Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr; 1955 Feb 19; 193(4):427-48. PubMed ID: 13249581
    [No Abstract] [Full Text] [Related]

  • 14. Muscular dystrophy in Northern Ireland. IV. Some additional data.
    STEVENSON AC.
    Ann Hum Genet; 1958 May 19; 22(3):231-4. PubMed ID: 13534208
    [No Abstract] [Full Text] [Related]

  • 15. Familial congenital muscular dystrophy with gonadal dysgenesis.
    BASSOE HH.
    J Clin Endocrinol Metab; 1956 Dec 19; 16(12):1614-21. PubMed ID: 13385309
    [No Abstract] [Full Text] [Related]

  • 16. Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.
    STEPHENS FE, TYLER FH.
    Am J Hum Genet; 1951 Jun 19; 3(2):111-25. PubMed ID: 14902757
    [No Abstract] [Full Text] [Related]

  • 17. [Dominant heredity of progressive muscular dystrophy in family in Vaud].
    JEQUIER M, HANHART E.
    Acta Neurol Psychiatr Belg; 1954 Feb 19; 54(2):120-7. PubMed ID: 13157966
    [No Abstract] [Full Text] [Related]

  • 18. Muscular dystrophy in Northern Ireland, I. An account of the condition in fifty-one families.
    STEVENSON AC.
    Ann Eugen; 1953 Jun 19; 17(1):50-93; contd. PubMed ID: 13058272
    [No Abstract] [Full Text] [Related]

  • 19. A case of myopathy.
    APPAJAPPA M, SHAMANNA D.
    J Indian Med Assoc; 1956 Sep 01; 27(5):182. PubMed ID: 13367446
    [No Abstract] [Full Text] [Related]

  • 20. [Combined transmission of three different hereditary diseases in the same family (deforming juvenile osteochondrosis of the hip, hypoplasia of the femur, progressive muscular dystrophy)].
    PFANDLER U.
    J Genet Hum; 1952 May 01; 1(1):56-82. PubMed ID: 12981241
    [No Abstract] [Full Text] [Related]

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