-
1
-
-
0027160266
-
Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia
-
Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakav AV, Lebedev VM, Kuznetzova TV, Shlykova SN, Mikhailov AV, Vakharlovsky VG (1993) Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia. Prenat Diagn 13 : 323-333
-
(1993)
Prenat Diagn
, vol.13
, pp. 323-333
-
-
Baranov, V.S.1
Gorbunova, V.N.2
Malysheva, O.V.3
Artemyeva, O.V.4
Kascheeva, T.K.5
Evgrafov, O.V.6
Polyakav, A.V.7
Lebedev, V.M.8
Kuznetzova, T.V.9
Shlykova, S.N.10
Mikhailov, A.V.11
Vakharlovsky, V.G.12
-
2
-
-
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
-
3
-
-
0002503692
-
Multiplex PCR for the diagnosis of Duchenne muscular dystrophy
-
Innis MA, Gelfald DW, Sninski JJ, White JJ (eds) Academic Press, New York
-
Chamberlain JS, Gibbs RA, Ranier JF, Caskey CT (1990) Multiplex PCR for the diagnosis of Duchenne muscular dystrophy. In: PCR protocols. A guide to methods and application. Innis MA, Gelfald DW, Sninski JJ, White JJ (eds) Academic Press, New York, pp 272-281
-
(1990)
PCR Protocols. A Guide to Methods and Application
, pp. 272-281
-
-
Chamberlain, J.S.1
Gibbs, R.A.2
Ranier, J.F.3
Caskey, C.T.4
-
4
-
-
0027195244
-
Patterns of deletions of the dystrophin gene in different European populations
-
Danieli GA, Mioni F, Muller CR, Vitiello L, Mostacciuolo ML, Grimm T (1993) Patterns of deletions of the dystrophin gene in different European populations. Hum Genet 91 : 342-346
-
(1993)
Hum Genet
, vol.91
, pp. 342-346
-
-
Danieli, G.A.1
Mioni, F.2
Muller, C.R.3
Vitiello, L.4
Mostacciuolo, M.L.5
Grimm, T.6
-
6
-
-
0028940944
-
Deletion patterns of Duchenne and Becker muscular dystrophies in Greece
-
Florentin L, Mavrou A, Kekou K, Metaxotou C (1994) Deletion patterns of Duchenne and Becker muscular dystrophies in Greece. J Med Genet 32 : 48-51
-
(1994)
J Med Genet
, vol.32
, pp. 48-51
-
-
Florentin, L.1
Mavrou, A.2
Kekou, K.3
Metaxotou, C.4
-
7
-
-
0027198597
-
Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR
-
Gokgoz N, Kuseyri F, Topaloglu H, Yuksel-Apak M, Kirdar B (1993) Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR. Clin Genet 43 : 261-266
-
(1993)
Clin Genet
, vol.43
, pp. 261-266
-
-
Gokgoz, N.1
Kuseyri, F.2
Topaloglu, H.3
Yuksel-Apak, M.4
Kirdar, B.5
-
8
-
-
0027092397
-
Quantitative Southern blot analysis in the dystrophin gene of Japanese patients with Duchenne or Becker muscular dystrophy: A high frequency of duplications
-
Hiraishi Y, Kato S, Ishihara T, Takano T (1992) Quantitative Southern blot analysis in the dystrophin gene of Japanese patients with Duchenne or Becker muscular dystrophy: a high frequency of duplications. J Med Genet 29 : 897-901
-
(1992)
J Med Genet
, vol.29
, pp. 897-901
-
-
Hiraishi, Y.1
Kato, S.2
Ishihara, T.3
Takano, T.4
-
9
-
-
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, Huffman 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
Huffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
10
-
-
0025762012
-
Gene deletions causing human genetic disease: Mechanisms of mutagenesis and the role of local DNA sequence environment
-
Krawczak M, Cooper DN (1991) Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence environment. Hum Genet 86 : 425-441
-
(1991)
Hum Genet
, vol.86
, pp. 425-441
-
-
Krawczak, M.1
Cooper, D.N.2
-
11
-
-
0024598162
-
Molecular deletion patterns in Duchenne and Becker type muscular dystrophies
-
Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H (1989) Molecular deletion patterns in Duchenne and Becker type muscular dystrophies. Hum Genet 81 : 343-348
-
(1989)
Hum Genet
, vol.81
, pp. 343-348
-
-
Liechti-Gallati, S.1
Koenig, M.2
Kunkel, L.M.3
Frey, D.4
Boltshauser, E.5
Schneider, V.6
Braga, S.7
Moser, H.8
-
12
-
-
0025847315
-
Sequence of junction fragments in the deletion prone region of the dystrophin gene
-
Love DR, England SB, Speer A, Marsden RF, Bloomfield JF, Roche AL, Cross GS, Mountfored RC, Smith TJ, Davies KE (1991) Sequence of junction fragments in the deletion prone region of the dystrophin gene. Genomics 10 : 56-67
-
(1991)
Genomics
, vol.10
, pp. 56-67
-
-
Love, D.R.1
England, S.B.2
Speer, A.3
Marsden, R.F.4
Bloomfield, J.F.5
Roche, A.L.6
Cross, G.S.7
Mountfored, R.C.8
Smith, T.J.9
Davies, K.E.10
-
13
-
-
0026793658
-
Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy
-
Niemann-Seyde S, Slomski R, Rininsland F, Ellermeyer U, Kwaitkowska 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
Kwaitkowska, J.5
Reiss, J.6
-
14
-
-
0028845255
-
Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals. Deletion detection and familial diagnosis
-
Patino A, Narbona J, Garcia-Delgado M (1995) Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals. Deletion detection and familial diagnosis. Am J Med Genet 59 : 182-187
-
(1995)
Am J Med Genet
, vol.59
, pp. 182-187
-
-
Patino, A.1
Narbona, J.2
Garcia-Delgado, M.3
-
15
-
-
0028610022
-
New clinical sign in Duchenne muscular dystrophy
-
Pradhan S (1994) New clinical sign in Duchenne muscular dystrophy. Pediatr Neurol 11 : 298-300
-
(1994)
Pediatr Neurol
, vol.11
, pp. 298-300
-
-
Pradhan, S.1
-
16
-
-
0026717934
-
Racial distribution of Duchenne muscular dystrophy in the West Midlands region of Britain
-
Roddie A, Bundey S (1992) Racial distribution of Duchenne muscular dystrophy in the West Midlands region of Britain. J Med Genet 29 : 555-557
-
(1992)
J Med Genet
, vol.29
, pp. 555-557
-
-
Roddie, A.1
Bundey, S.2
-
17
-
-
0028084292
-
Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients
-
Shomrat R, Gluck E, Legum C, Shiloh Y (1994) Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. Am J Med Genet 49 : 369-373
-
(1994)
Am J Med Genet
, vol.49
, pp. 369-373
-
-
Shomrat, R.1
Gluck, E.2
Legum, C.3
Shiloh, Y.4
-
18
-
-
0030461581
-
High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patients
-
in press
-
Sinha S, Mishra S, Singh V, Mittal RD, Mittal B (1996) High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patients. Clin Genet (in press)
-
(1996)
Clin Genet
-
-
Sinha, S.1
Mishra, S.2
Singh, V.3
Mittal, R.D.4
Mittal, B.5
-
19
-
-
0026062480
-
DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese
-
Soong B-W, Tsai T-F, Su C-H, Kao K-P, Hsiao K-J, Su T-S (1991) DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese. Am J Med Genet 38 : 593-600
-
(1991)
Am J Med Genet
, vol.38
, pp. 593-600
-
-
Soong, B.-W.1
Tsai, T.-F.2
Su, C.-H.3
Kao, K.-P.4
Hsiao, K.-J.5
Su, T.-S.6
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