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journal-article
BMJ
Journal of Medical Genetics (239)
References
39
Referenced
63
- l Dubowitz V. Mental retardation in Duchenne muscular dystrophy. In: Pathogenesis of human muscular dystrophies. Excerpta Medica international congress series 404. Amsterdam: Excerpta Medica, 1976:689-94. / Mental retardation in Duchenne muscular dystrophy. In: Pathogenesis of human muscular dystrophies. Excerpta Medica international congress series 404 by l Dubowitz V (1976)
- Emery AEH. In: Duchenne muscular dystrophy. Oxford monographs in medical genetics No 15. Oxford: Oxford University Press, 1987:99-102. / Oxford monographs in medical genetics No 15 / In: Duchenne muscular dystrophy by Emery, A.E.H. (1987)
-
Emery AEH, Skinner R. Clinical studies in benign (Becker type) X-linked muscular dystrophy. Clin Genet 1976;10:189-201.
(
10.1111/j.1399-0004.1976.tb00033.x
) / Clin Genet / Clinical studies in benign (Becker type) X-linked muscular dystrophy by Emery, A.E.H.; Skinner, R. (1976) -
Davies KE, Pearson PL, Harper PS, et al. Linkage analysis of two cloned DNA sequences flanking the DMD locus on the short arm of the human X chromosome. Nucleic Acids Res 1983;11:2303-12.
(
10.1093/nar/11.8.2303
) / Nucleic Acids Res / Linkage analysis of two cloned DNA sequences flanking the DMD locus on the short arm of the human X chromosome by Davies, K.E.; Pearson, P.L.; Harper, P.S. (1983) -
Kingston HM, Sarfarazi M, Thomas NST, Harper PS. Localisation of the BMD gene on the short arm of the X chromosome by linkage to cloned DNA sequences. Hum Genet 1984;67:6-17.
(
10.1007/BF00270551
) / Hum Genet / Localisation of the BMD gene on the short arm of the X chromosome by linkage to cloned DNA sequences by Kingston, H.M.; Sarfarazi, M.; Thomas, N.S.T.; Harper, P.S. (1984) -
Kunkel LM, Monaco AP, Middlesworth W, Ochs HD, Latt SA. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc Natl Acad Sci USA 1985;82:4778-82.
(
10.1073/pnas.82.14.4778
) / Proc Natl Acad Sci USA / Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion by Kunkel, L.M.; Monaco, A.P.; Middlesworth, W.; Ochs, H.D.; Latt, S.A. (1985) -
Ray PN, Belfall B, Duff C, et al. Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy. Nature 1985;318:672-5.
(
10.1038/318672a0
) / Nature / Cloning of the breakpoint of an X; 21 translocation associated with Duchenne muscular dystrophy by Ray, P.N.; Belfall, B.; Duff, C. (1985) -
Kunkel LM, Hejtmancik JF, Caskey CT, et al. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 1986;322:73-7.
(
10.1038/322073a0
) / Nature / Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy by Kunkel, L.M.; Hejtmancik, J.F.; Caskey, C.T. (1986) -
Hart KA, Hodgson S, Walker A, et al. DNA deletions in mild and severe Becker muscular dystrophy. Hum Genet 1987;75: 281-5.
(
10.1007/BF00281075
) / Hum Genet / DNA deletions in mild and severe Becker muscular dystrophy by Hart, K.A.; Hodgson, S.; Walker, A. (1987) -
Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM. Isolation of candidate cDNA for portions of the DMD gene. Nature 1986;323:646-50.
(
10.1038/323646a0
) / Nature / Isolation of candidate cDNA for portions of the DMD gene by Monaco, A.P.; Neve, R.L.; Colletti-Feener, C.; Bertelson, C.J.; Kurnit, D.M.; Kunkel, L.M. (1986) -
Burghes AHM, Logan C, Hu X, Belfall B, Worton RG, Ray PN. A cDNA clone from the D/BMD gene. Nature 1987;328: 434-7.
(
10.1038/328434a0
) / Nature / A cDNA clone from the D/BMD gene by Burghes, A.H.M.; Logan, C.; Hu, X.; Belfall, B.; Worton, R.G.; Ray, P.N. (1987) -
Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Burn J, Davies KE. Preferential deletion of exons in Duchenne and Becker muscular dystrophies. Nature 1987;329:638-40.
(
10.1038/329638a0
) / Nature / Preferential deletion of exons in Duchenne and Becker muscular dystrophies by Forrest, S.M.; Cross, G.S.; Speer, A.; Gardner-Medwin, D.; Burn, J.; Davies, K.E. (1987) -
Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 1987;50:509-17.
(
10.1016/0092-8674(87)90504-6
) / Cell / Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals by Koenig, M.; Hoffman, E.P.; Bertelson, C.J.; Monaco, A.P.; Feener, C.; Kunkel, L.M. (1987) -
Smith TJ, Forrest SM, Cross GS, Davies KE. Duchenne and Becker muscular dystrophy mutations: analysis using 2-6 kb of muscle cDNA from the 5' end of the gene. Nucleic Acids Res 1987;15:9761-9.
(
10.1093/nar/15.23.9761
) / Nucleic Acids Res / Duchenne and Becker muscular dystrophy mutations: analysis using 2-6 kb of muscle cDNA from the 5' end of the gene by Smith, T.J.; Forrest, S.M.; Cross, G.S.; Davies, K.E. (1987) -
Forrest SM, Cross GS, Flint T, Speer A, Robson KJH, Davies KE. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophy. Genomics 1988;2:109-14.
(
10.1016/0888-7543(88)90091-2
) / Genomics / Further studies of gene deletions that cause Duchenne and Becker muscular dystrophy by Forrest, S.M.; Cross, G.S.; Flint, T.; Speer, A.; Robson, K.J.H.; Davies, K.E. (1988) -
Koenig M, Monaco AP, Kunkel LM. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell 1988;53:219-28.
(
10.1016/0092-8674(88)90383-2
) / Cell / The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein by Koenig, M.; Monaco, A.P.; Kunkel, L.M. (1988) -
Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 1988;2:90-5.
(
10.1016/0888-7543(88)90113-9
) / Genomics / An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus by Monaco, A.P.; Bertelson, C.J.; Liechti-Gallati, S.; Moser, H.; Kunkel, L.M. (1988) - Brown RH, Hoffman EP. Molecular biology of Duchenne muscular dystrophy. Trends Genet 1988;11:480-4. / Trends Genet / Molecular biology of Duchenne muscular dystrophy by Brown, R.H.; Hoffman, E.P. (1988)
-
Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Da-vies KE, Harris R. Patterns of exon deletions in Duchenne and Becker muscular dystrophy. Hum Genet 1988;80:152-6.
(
10.1007/BF00702859
) / Hum Genet / Patterns of exon deletions in Duchenne and Becker muscular dystrophy by Read, A.P.; Mountford, R.C.; Forrest, S.M.; Kenwrick, S.J.; Da-vies, K.E.; Harris, R. (1988) -
Hoffman EP, Fischbeck KH, Brown RH, et al. Characterisation of dystrophin in muscle biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy. N Engl J Med 1988;318:1363-8.
(
10.1056/NEJM198805263182104
) / N Engl J Med / Characterisation of dystrophin in muscle biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy by Hoffman, E.P.; Fischbeck, K.H.; Brown, R.H. (1988) -
Malhotra SB, Hart KA, Klamut HJ, et al. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy. Science 1988;242:755-9.
(
10.1126/science.3055295
) / Science / Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy by Malhotra, S.B.; Hart, K.A.; Klamut, H.J. (1988) -
Nudel U, Robzyk K, Yaffe D. Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain. Nature 1988;331:635-8.
(
10.1038/331635a0
) / Nature / Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain by Nudel, U.; Robzyk, K.; Yaffe, D. (1988) -
Nudel I, Zuk D, Einat P, et al. Duchenne muscular dystrophy gene product is not identical in muscle and brain. Nature 1989;337:76-8.
(
10.1038/337076a0
) / Nature / Duchenne muscular dystrophy gene product is not identical in muscle and brain by Nudel, I.; Zuk, D.; Einat, P. (1989) - Dubowitz V. In: Muscle disorders in childhood. Major problems in clinical paediatrics Vol XVL. Philadelphia: Saunders, 1978: 31-6. / In: Muscle disorders in childhood. Major problems in clinical paediatrics Vol XVL by Dubowitz, V. (1978)
-
Heckmatt JZ, Dubowitz VG, Hyde SA, Florence J, Gabain AC, Thompson N. Prolongation of walking in DMD with lightweight orthoses: review of 57 cases. Dev Med Child Neurol 1985;27: 149-54.
(
10.1111/j.1469-8749.1985.tb03763.x
) / Dev Med Child Neurol / Prolongation of walking in DMD with lightweight orthoses: review of 57 cases by Heckmatt, J.Z.; Dubowitz, V.G.; Hyde, S.A.; Florence, J.; Gabain, A.C.; Thompson, N. (1985) - Illingworth RS. The development of the infant and young child-normal and abnormal. 5th ed. Edinburgh: Churchill Livingstone, 1974:1534. / The development of the infant and young child-normal and abnormal by Illingworth, R.S.
- Kunkel LM, Smith KD, Boyer SH, et al. Analysis of human Ychromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 1977,74:1245-9. / DNA in chromosome variants. Proc Natl Acad Sci USA / Analysis of human Ychromosome-specific reiterated by Kunkel, L.M.; Smith, K.D.; Boyer, S.H.
- Maniatis T, Fritsch CF, Sanbrook J, eds. Molecular cloning: a laboratory manual. Cold Spring Harbor, New York:, Cold Spring Harbor Laboratories, 1982. / Cold Spring Harbor, New York:, Cold Spring Harbor Laboratories / Molecular cloning: a laboratory manual by Maniatis, T. (1982)
-
Feinberg AP, Vogelstein B. A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 1983;132:6-13.
(
10.1016/0003-2697(83)90418-9
) / Anal Biochem / A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity by Feinberg, A.P.; Vogelstein, B. (1983) - Burghes AHM, Duff C, Hart KA, et al. Exons deleted and duplicated in Becker and Duchenne muscular dystrophy at the 5' end of the DMD gene. (In preparation). 3' Wapenaar MC, Kievits T, Hart KA, et al. A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics 1988;2: 101-8. / Genomics; A deletion hot spot in the Duchenne muscular dystrophy gene / Exons deleted and duplicated in Becker and Duchenne muscular dystrophy at the 5' end of the DMD gene. (In preparation). 3' by Burghes, A.H.M.; Duff, C.; Hart, K.A. (1988)
-
Hart KA, Abbs S, Wapenaar MC, Cole CG, Hodgson SV, Bobrow M. Molecular deletions in the Duchenne/Becker muscular dystrophy gene. Clin Genet 1989;35:251-60.
(
10.1111/j.1399-0004.1989.tb02939.x
) / Clin Genet / Molecular deletions in the Duchenne/Becker muscular dystrophy gene by Hart, K.A.; Abbs, S.; Wapenaar, M.C.; Cole, C.G.; Hodgson, S.V.; Bobrow, M. (1989) - Hart KA. Molecular deletions in the DuchennelBecker muscular dystrophy locus. PhD thesis, University of London, 1989. / Molecular deletions in the DuchennelBecker muscular dystrophy locus by Hart, K.A. (1989)
- Determination of the power of therapeutic trials based on the natural history. Muscle Nerve 1983; February:91-103. 35 Hyser CL, Province M, Griggs RC, et al. Genetic heterogeneity in Duchenne dystrophy. Ann Neurol 1987;22:411-20. 3 Darras BT, Blattner P, Harper JF, Spiro AJ, Alter S, Francke U. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglIl exon-containing fragment maps, meiotic and mitotic origin of the mutations. Am J Hum Genet 1988;43:620-9. / Genetic heterogeneity in Duchenne dystrophy; Ann Neurol / Determination of the power of therapeutic trials based on the natural history by Hyser, C.L.; Province, M.; Griggs, R.C. (1983)
-
Hammonds RG. Protein sequence of DMD is related to actinbinding domain of ct-actinin. Cell 1988;51:1.
(
10.1016/0092-8674(87)90002-X
) / Cell / Protein sequence of DMD is related to actinbinding domain of ct-actinin by Hammonds, R.G. (1988) -
Cooper BJ, Winand NJ, Stedman H, et al. The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs. Nature 1988;334:154-6.
(
10.1038/334154a0
) / Nature / The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs by Cooper, B.J.; Winand, N.J.; Stedman, H. (1988) - Prosser EJ, Murphy EG, Thompson MW. Intelligence and the gene for Duchenne muscular dystrophy. Arch Dis Child 1969;44:221-30. 4() Miller G, Tunnecliffe M, Douglas PS. IQ, prognosis, and Duchenne muscular dystrophy. Brain Dev 1985;7:7-9. / Arch Dis Child; PS. IQ, prognosis, and Duchenne muscular dystrophy / Intelligence and the gene for Duchenne muscular dystrophy by Prosser, E.J.; Murphy, E.G.; Thompson, M.W. (1985)
-
Rabbi-Bortolini E, Zatz M. Investigations on genetic heterogeneity in Duchenne muscular dystrophy. Am J Med Genet 1986;24: 111-7.
(
10.1002/ajmg.1320240113
) / Am J Med Genet / Investigations on genetic heterogeneity in Duchenne muscular dystrophy by Rabbi-Bortolini, E.; Zatz, M. (1986) -
Zatz M, Betti RTB, Levy J. Benign Duchenne muscular dystrophy in a patient with growth hormone deficiency. Am J Med Genet 1981;10:301-4.
(
10.1002/ajmg.1320100313
) / Am J Med Genet / Benign Duchenne muscular dystrophy in a patient with growth hormone deficiency by Zatz, M.; Betti, R.T.B.; Levy, J. (1981) -
Eiholzer U, Boltshauser E, Frey D, Molinari L, Zachmann M. Short stature: a common feature in Duchenne muscular dystrophy. Eur J Pediatr 1988;147:602-5.
(
10.1007/BF00442472
) / Eur J Pediatr / Short stature: a common feature in Duchenne muscular dystrophy by Eiholzer, U.; Boltshauser, E.; Frey, D.; Molinari, L.; Zachmann, M. (1988)
Dates
Type | When |
---|---|
Created | 16 years, 9 months ago (Nov. 10, 2008, 3:11 p.m.) |
Deposited | 1 year, 6 months ago (March 2, 2024, 6:07 a.m.) |
Indexed | 11 months, 3 weeks ago (Sept. 15, 2024, 6:34 a.m.) |
Issued | 35 years, 10 months ago (Nov. 1, 1989) |
Published | 35 years, 10 months ago (Nov. 1, 1989) |
Published Print | 35 years, 10 months ago (Nov. 1, 1989) |
@article{Hodgson_1989, title={Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.}, volume={26}, ISSN={1468-6244}, url={http://dx.doi.org/10.1136/jmg.26.11.682}, DOI={10.1136/jmg.26.11.682}, number={11}, journal={Journal of Medical Genetics}, publisher={BMJ}, author={Hodgson, S and Hart, K and Abbs, S and Heckmatt, J and Rodillo, E and Bobrow, M and Dubowitz, V}, year={1989}, month=nov, pages={682–693} }