-
1
-
-
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
-
2
-
-
0025719080
-
242 breakpoints in the 200-kb deletion prone p20 region of the DMD gene are widely spread
-
Blonden LAJ, Grootscholten PM, Den Dunnen JT, Bakker E, Abbs S, Bobrow M, Boehm C, Van Broeckoven C, Baumback L, Chamberlain J, Caskey CT, Denton M, Felicetti L, Galluzzi G, Fishbeck KH, et al. (1991) 242 breakpoints in the 200-kb deletion prone p20 region of the DMD gene are widely spread. Genomics 10:631-639
-
(1991)
Genomics
, vol.10
, pp. 631-639
-
-
Blonden, L.A.J.1
Grootscholten, P.M.2
Den Dunnen, J.T.3
Bakker, E.4
Abbs, S.5
Bobrow, M.6
Boehm, C.7
Van Broeckoven, C.8
Baumback, L.9
Chamberlain, J.10
Caskey, C.T.11
Denton, M.12
Felicetti, L.13
Galluzzi, G.14
Fishbeck, K.H.15
-
3
-
-
0030588069
-
Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3
-
Brown J, Dry KL, Edgar AJ, Pryde FE, Hardwick LJ, Aldred MA, Lester DH, Boyle S, Kaplan J, Dufier JL, Ho MF, Monaco AP, Musarella MA, Wright AF (1996) Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3. Genomics 37:200-210
-
(1996)
Genomics
, vol.37
, pp. 200-210
-
-
Brown, J.1
Dry, K.L.2
Edgar, A.J.3
Pryde, F.E.4
Hardwick, L.J.5
Aldred, M.A.6
Lester, D.H.7
Boyle, S.8
Kaplan, J.9
Dufier, J.L.10
Ho, M.F.11
Monaco, A.P.12
Musarella, M.A.13
Wright, A.F.14
-
4
-
-
0023046824
-
A calculation of fragment lengths obtainable from human DNA with 78 restriction enzymes: An aid for cloning and mapping
-
Drmanac R, Petrovic N, Glisin V, Crkvenjakov R (1986) A calculation of fragment lengths obtainable from human DNA with 78 restriction enzymes: An aid for cloning and mapping. Nucleic Acids Res 14:4691-4692
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 4691-4692
-
-
Drmanac, R.1
Petrovic, N.2
Glisin, V.3
Crkvenjakov, R.4
-
5
-
-
0024815723
-
Topography of Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveal 115 deletions and 13 duplications
-
Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LAJ, Ginjar HB, Wapenaar MC, Van Passen HMB, Van Broeckhonen C, Pearson PL, Van Ommen GJB (1989) Topography of Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveal 115 deletions and 13 duplications. Am J Hum Genet 45:835-847
-
(1989)
Am J Hum Genet
, vol.45
, pp. 835-847
-
-
Den Dunnen, J.T.1
Grootscholten, P.M.2
Bakker, E.3
Blonden, L.A.J.4
Ginjar, H.B.5
Wapenaar, M.C.6
Van Passen, H.M.B.7
Van Broeckhonen, C.8
Pearson, P.L.9
Van Ommen, G.J.B.10
-
7
-
-
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, Betteken T, Meng G, Muller CR, Lindlof M, Kaariainen H, De La Chapelle A, Kiuru A, Savontaus ML, Gilkenkranz H, Recan D, et al (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
Betteken, 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
Gilkenkranz, H.14
Recan, D.15
-
8
-
-
0025847315
-
Sequences 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, Mountford RC, Smith TJ, Davies KE (1991) Sequences of junction fragments in the deletion-prone region of the dystrophin gene. Genomics 10:57-67
-
(1991)
Genomics
, vol.10
, pp. 57-67
-
-
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
Mountford, R.C.8
Smith, T.J.9
Davies, K.E.10
-
9
-
-
0032487761
-
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene
-
McNaughton JC, Cockburn DJ, Hughes G, Jones WA, Laing NG, Ray PN, Stockwell PA, Petersen GB (1998) Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene. Gene 222:411-51
-
(1998)
Gene
, vol.222
, pp. 411-451
-
-
McNaughton, J.C.1
Cockburn, D.J.2
Hughes, G.3
Jones, W.A.4
Laing, N.G.5
Ray, P.N.6
Stockwell, P.A.7
Petersen, G.B.8
-
10
-
-
0030700474
-
Exon-intron organization of the human dystrophin gene
-
Nobile C, Marchi J, Nigro V, Roberts RG, Danieli GA (1997) Exon-intron organization of the human dystrophin gene. Genomics 45:421-424
-
(1997)
Genomics
, vol.45
, pp. 421-424
-
-
Nobile, C.1
Marchi, J.2
Nigro, V.3
Roberts, R.G.4
Danieli, G.A.5
-
11
-
-
0035680324
-
The HUGO Gene Nomenclature Committee (HGNC)
-
DOI 101007/s00439-001-0615-0
-
Povey S, Lovering R, Bruford E, Wright M, Lush M, Wain H (2001) The HUGO Gene Nomenclature Committee (HGNC). Hum Genet DOI 101007/s00439-001-0615-0
-
(2001)
Hum Genet
-
-
Povey, S.1
Lovering, R.2
Bruford, E.3
Wright, M.4
Lush, M.5
Wain, H.6
-
12
-
-
0026714803
-
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR
-
Roberts RG, Coffey AG, Bobrow M, Bentley DR (1992) Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR. Genomics 13:942-950
-
(1992)
Genomics
, vol.13
, pp. 942-950
-
-
Roberts, R.G.1
Coffey, A.G.2
Bobrow, M.3
Bentley, D.R.4
-
13
-
-
0030741634
-
Mathematical model to predict regions of chromatin attachment to the nuclear matrix
-
Singh GB, Kramer JA, Krawetz SA (1997) Mathematical model to predict regions of chromatin attachment to the nuclear matrix. Nucleic Acids Res 25:1419-1425
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 1419-1425
-
-
Singh, G.B.1
Kramer, J.A.2
Krawetz, S.A.3
|