-
1
-
-
0027470203
-
The structural and functional diversity of dystrophin
-
Ahn AH, Kunkel LM (1993) The structural and functional diversity of dystrophin. Nat Genet 3:283-291
-
(1993)
Nat Genet
, vol.3
, pp. 283-291
-
-
Ahn, A.H.1
Kunkel, L.M.2
-
2
-
-
0027936884
-
Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected
-
Ballo R, Viljoen D, Beighton P (1994) Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected. S Afr Med J 84:494-497
-
(1994)
S Afr Med J
, vol.84
, pp. 494-497
-
-
Ballo, R.1
Viljoen, D.2
Beighton, P.3
-
3
-
-
0031049169
-
Are there ethnic differences in deletions in the dystrophin gene?
-
Banerjee M, Verma IC (1997) Are there ethnic differences in deletions in the dystrophin gene? Am J Med Genet 68:152-157
-
(1997)
Am J Med Genet
, vol.68
, pp. 152-157
-
-
Banerjee, M.1
Verma, I.C.2
-
4
-
-
0024580404
-
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies
-
Baumbach LL, Chamberlain JS, Ward PA, Farwell NJ, Caskey CT (1989) Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies. Neurology 39:465-474
-
(1989)
Neurology
, vol.39
, pp. 465-474
-
-
Baumbach, L.L.1
Chamberlain, J.S.2
Ward, P.A.3
Farwell, N.J.4
Caskey, C.T.5
-
5
-
-
0025244924
-
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
-
Beggs AH, Koenig M, Boyce FM, Kunkel LM (1990) Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet 86:45-48
-
(1990)
Hum Genet
, vol.86
, pp. 45-48
-
-
Beggs, A.H.1
Koenig, M.2
Boyce, F.M.3
Kunkel, L.M.4
-
6
-
-
0024245082
-
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
-
Chamberlain JS, Gibbs RA, Ranier JE, Nguyen PN, Caskey CT (1988) Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res 16:11141-11156
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 11141-11156
-
-
Chamberlain, J.S.1
Gibbs, R.A.2
Ranier, J.E.3
Nguyen, P.N.4
Caskey, C.T.5
-
7
-
-
0025738298
-
Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene
-
Covone AE, Lerone ML, Romeo G (1991) Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene. Hum Genet 87:353-360
-
(1991)
Hum Genet
, vol.87
, pp. 353-360
-
-
Covone, A.E.1
Lerone, M.L.2
Romeo, G.3
-
8
-
-
0029638066
-
More deletions in the 5′ region than in the central region of the dystrophin gene were identified among Filipino Duchenne and Becker muscular dystrophy patients
-
Cutiongco EM, Padilla CD, Takenaka K, Yamasaki Y, Nishio H, Matsuo M (1995) More deletions in the 5′ region than in the central region of the dystrophin gene were identified among Filipino Duchenne and Becker muscular dystrophy patients. Am J Med Genet 59:266-267
-
(1995)
Am J Med Genet
, vol.59
, pp. 266-267
-
-
Cutiongco, E.M.1
Padilla, C.D.2
Takenaka, K.3
Yamasaki, Y.4
Nishio, H.5
Matsuo, M.6
-
9
-
-
0343396715
-
Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients
-
Dincer P, Topaloglu H, Ayter S, Ozguc M, Tasdemir HA, Renda Y (1996) Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. Brain Dev 18:91-94
-
(1996)
Brain Dev
, vol.18
, pp. 91-94
-
-
Dincer, P.1
Topaloglu, H.2
Ayter, S.3
Ozguc, M.4
Tasdemir, H.A.5
Renda, Y.6
-
10
-
-
0023957073
-
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
-
Forrest SM, Cross GS, Flint T, Speer A, Robson KJH, Davies KE (1988) Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies. Genomics 2:109-114
-
(1988)
Genomics
, vol.2
, pp. 109-114
-
-
Forrest, S.M.1
Cross, G.S.2
Flint, T.3
Speer, A.4
Robson, K.J.H.5
Davies, K.E.6
-
11
-
-
0024430346
-
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene
-
Gillard EF, Chamberlain JS, Murphy EG, Duff CL, Smith B, Burghes AH, Thompson MW, Sutherland J, Oss I, Bodrug SE, Klamut HJ, Ray PN, Worton RG (1989) Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene. Am J Hum Genet 45:507-520
-
(1989)
Am J Hum Genet
, vol.45
, pp. 507-520
-
-
Gillard, E.F.1
Chamberlain, J.S.2
Murphy, E.G.3
Duff, C.L.4
Smith, B.5
Burghes, A.H.6
Thompson, M.W.7
Sutherland, J.8
Oss, I.9
Bodrug, S.E.10
Klamut, H.J.11
Ray, P.N.12
Worton, R.G.13
-
12
-
-
0345580874
-
Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
-
Herczegfalvi A, Toth G, Gyurus P, Morava E, Endreffy E, Fodor F, Mechler F, Laszlo A, Rasko I, Melegh B (1999) Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies. Neuromuscul Disord 9:552-554
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 552-554
-
-
Herczegfalvi, A.1
Toth, G.2
Gyurus, P.3
Morava, E.4
Endreffy, E.5
Fodor, F.6
Mechler, F.7
Laszlo, A.8
Rasko, I.9
Melegh, B.10
-
13
-
-
0024332141
-
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
-
Hoffman EP, Kunkel LM (1989) Dystrophin abnormalities in Duchenne/Becker muscular dystrophy. Neuron 2:1019-1029
-
(1989)
Neuron
, vol.2
, pp. 1019-1029
-
-
Hoffman, E.P.1
Kunkel, L.M.2
-
14
-
-
0031955191
-
Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis
-
Ikezawa M, Minami N, Takahashi M, Goto Y, Miike T, Nonaka I (1998) Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis. Brain Dev 20:165-168
-
(1998)
Brain Dev
, vol.20
, pp. 165-168
-
-
Ikezawa, M.1
Minami, N.2
Takahashi, M.3
Goto, Y.4
Miike, T.5
Nonaka, I.6
-
15
-
-
0028420822
-
Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA
-
Kitoh Y, Matsuo M, Nishio H, Nakamura H (1994) Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA. Kobe J Med Sci 40:39-48
-
(1994)
Kobe J Med Sci
, vol.40
, pp. 39-48
-
-
Kitoh, Y.1
Matsuo, M.2
Nishio, H.3
Nakamura, H.4
-
16
-
-
0023614271
-
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
-
Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509-517
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
Hoffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
17
-
-
0024466501
-
The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion
-
Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Muller CR, Lindlof M, Kaariainen H, de la Chapelle A, Kiuru A, Savontaus M-L, Gilgenkrantz H, Recan D, Chelly J, Kaplan J-C, Covone AE, Archidiacono N, Romeo G, Liechti-Gallati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LAJ, van Paassen HMB, van Ommen GJB, Kunkel LM (1989) The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion. Am J Hum Genet 45:498-506
-
(1989)
Am J Hum Genet
, vol.45
, pp. 498-506
-
-
Koenig, M.1
Beggs, A.H.2
Moyer, M.3
Scherpf, S.4
Heindrich, K.5
Bettecken, T.6
Meng, G.7
Muller, C.R.8
Lindlof, M.9
Kaariainen, H.10
De la Chapelle, A.11
Kiuru, A.12
Savontaus, M.-L.13
Gilgenkrantz, H.14
Recan, D.15
Chelly, J.16
Kaplan, J.-C.17
Covone, A.E.18
Archidiacono, N.19
Romeo, G.20
Liechti-Gallati, S.21
Schneider, V.22
Braga, S.23
Moser, H.24
Darras, B.T.25
Murphy, P.26
Francke, U.27
Chen, J.D.28
Morgan, G.29
Denton, M.30
Greenberg, C.R.31
Wrogemann, K.32
Blonden, L.A.J.33
Van Paassen, H.M.B.34
Van Ommen, G.J.B.35
Kunkel, L.M.36
more..
-
18
-
-
0032151218
-
Molecular-genetic characteristics of mutations in dystrophin gene and clinical symptoms in Duchenne muscular dystrophy
-
Lisiecka D, Wigowska-Sowinska J, Kwiatkowska J, Galas-Zgorzalewicz B, Slomski R (1998) Molecular-genetic characteristics of mutations in dystrophin gene and clinical symptoms in Duchenne muscular dystrophy. Neurol Neurochir Pol 32:1069-1079
-
(1998)
Neurol Neurochir Pol
, vol.32
, pp. 1069-1079
-
-
Lisiecka, D.1
Wigowska-Sowinska, J.2
Kwiatkowska, J.3
Galas-Zgorzalewicz, B.4
Slomski, R.5
-
19
-
-
0023718118
-
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
-
Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM (1988) An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2:90-95
-
(1988)
Genomics
, vol.2
, pp. 90-95
-
-
Monaco, A.P.1
Bertelson, C.J.2
Liechti-Gallati, S.3
Moser, H.4
Kunkel, L.M.5
-
20
-
-
0029377697
-
Multiplex PCR to detect the dystrophin gene deletion in Thai patients
-
Mutirangura A, Jongpiputvanich S, Norapucsunton T, Theamboonlers A, Srivuthana S, Promchainant C, Tumwasorn S, Sueblinvong T (1995) Multiplex PCR to detect the dystrophin gene deletion in Thai patients. J Med Assoc Thai 78:460-465
-
(1995)
J Med Assoc Thai
, vol.78
, pp. 460-465
-
-
Mutirangura, A.1
Jongpiputvanich, S.2
Norapucsunton, T.3
Theamboonlers, A.4
Srivuthana, S.5
Promchainant, C.6
Tumwasorn, S.7
Sueblinvong, T.8
-
21
-
-
0026793658
-
Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy
-
Niemann-Seyde S, Slomski R, Rininsland F, Ellermeyer U, Kwiatkowska J, Reiss J (1992) Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy. Hum. Genet. 90:65-70
-
(1992)
Hum Genet
, vol.90
, pp. 65-70
-
-
Niemann-Seyde, S.1
Slomski, R.2
Rininsland, F.3
Ellermeyer, U.4
Kwiatkowska, J.5
Reiss, J.6
-
22
-
-
0035479196
-
Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients
-
Werneck LC, Scola RH, Maegawa GH, Werneck MC (2001) Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients. Am J Med Genet 103:115-120
-
(2001)
Am J Med Genet
, vol.103
, pp. 115-120
-
-
Werneck, L.C.1
Scola, R.H.2
Maegawa, G.H.3
Werneck, M.C.4
-
23
-
-
0033597809
-
Detection of gene deletions in Chinese patients with Duchenne/Becker muscular dystrophy using cDNA probes and the polymerase chain reaction method
-
Yuge L, Hui L, Bingdi X (1999) Detection of gene deletions in Chinese patients with Duchenne/Becker muscular dystrophy using cDNA probes and the polymerase chain reaction method. Life Sci 65:863-869
-
(1999)
Life Sci
, vol.65
, pp. 863-869
-
-
Yuge, L.1
Hui, L.2
Bingdi, X.3
|