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Journal Abstract Search

173 related items for PubMed ID: 2732990

  • 1. Benign muscular dystrophy: risk calculation in families with consanguinity.
    Wolff G, Müller CR, Grimm T.
    J Med Genet; 1989 May; 26(5):299-304. PubMed ID: 2732990
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May; 103(1):65-75. PubMed ID: 1865235
    [Abstract] [Full Text] [Related]

  • 4. Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.
    Kingston HM, Sarfarazi M, Newcombe RG, Willis N, Harper PS.
    Clin Genet; 1985 Apr; 27(4):383-91. PubMed ID: 3995787
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
    [Abstract] [Full Text] [Related]

  • 8. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE, Strehler DA.
    Pediatrics; 1968 Feb 04; 41(2):495-502. PubMed ID: 5637795
    [No Abstract] [Full Text] [Related]

  • 9. 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 04; 25(2):211-8. PubMed ID: 3777018
    [Abstract] [Full Text] [Related]

  • 10. [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 Oct 04; 38(1):23-33. PubMed ID: 7284070
    [Abstract] [Full Text] [Related]

  • 11. [Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy].
    Janka M, Grimm T.
    Klin Padiatr; 1991 Oct 04; 203(5):354-8. PubMed ID: 1942941
    [Abstract] [Full Text] [Related]

  • 12. [Genetics of muscular dystrophies].
    Harper PS.
    Recenti Prog Med; 1977 May 04; 62(5):489-511. PubMed ID: 329369
    [No Abstract] [Full Text] [Related]

  • 13. Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.
    Suthers GK, Manson JI, Stern LM, Haan EA, Mulley JC.
    J Med Genet; 1989 Apr 04; 26(4):251-4. PubMed ID: 2716035
    [Abstract] [Full Text] [Related]

  • 14. X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.
    Kaladhar Reddy B, Anandavalli TE, Reddi OS.
    Hum Genet; 1984 Apr 04; 67(4):460-2. PubMed ID: 6490012
    [Abstract] [Full Text] [Related]

  • 15. Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
    Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A.
    Clin Genet; 1990 Mar 04; 37(3):179-87. PubMed ID: 1969777
    [Abstract] [Full Text] [Related]

  • 16. Becker-like muscular dystrophy in sisters.
    Diószeghy P, Molnár M, Mechler F.
    Eur Arch Psychiatry Clin Neurosci; 1995 Mar 04; 245(6):326-30. PubMed ID: 8527470
    [Abstract] [Full Text] [Related]

  • 17. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A.
    J Med Genet; 1986 Dec 04; 23(6):560-72. PubMed ID: 2879928
    [Abstract] [Full Text] [Related]

  • 18. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
    Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Jan 04; 317(1):70-6. PubMed ID: 7987694
    [Abstract] [Full Text] [Related]

  • 19. The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.
    Skinner R, Emery AE, Anderson AJ, Foxall C.
    J Med Genet; 1975 Jun 04; 12(2):131-4. PubMed ID: 1142377
    [No Abstract] [Full Text] [Related]

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