-
1
-
-
0031049169
-
Are there ethnic differences in deletions in the dystrophin gene?
-
Banerjee, M. & Verma, I. C. (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
-
2
-
-
0026801550
-
DNA analysis in Turkish Duchenne/Becker muscular dystrophy families
-
Battaloǧlu, E., Telatar, M., Deymeer, F., Serdaroǧlu, P., Kuseyri, F., Özdemir, C., Apak, M. & Tolun, A. (1992). DNA analysis in Turkish Duchenne/Becker muscular dystrophy families. Hum. Genet. 89, 635-639.
-
(1992)
Hum. Genet.
, vol.89
, pp. 635-639
-
-
Battaloǧlu, E.1
Telatar, M.2
Deymeer, F.3
Serdaroǧlu, P.4
Kuseyri, F.5
Özdemir, C.6
Apak, M.7
Tolun, A.8
-
3
-
-
0025244924
-
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
-
Beggs, A. H., Koenig, M., Boyce, F. M. & Kunkel L. M. (1990). Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum. Genet. 86, 40-48.
-
(1990)
Hum. Genet.
, vol.86
, pp. 40-48
-
-
Beggs, A.H.1
Koenig, M.2
Boyce, F.M.3
Kunkel, L.M.4
-
4
-
-
0030058638
-
From asia to Europe: Mitochondrial DNA sequence variability in Bulgarians and Turks
-
Calafell, F., Underhill, P., Tolun, A., Angelicheva, D. & Kalaydjieva, L. (1996). From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks. Ann. Hum. Genet. 60, 35-49.
-
(1996)
Ann. Hum. Genet.
, vol.60
, pp. 35-49
-
-
Calafell, F.1
Underhill, P.2
Tolun, A.3
Angelicheva, D.4
Kalaydjieva, L.5
-
6
-
-
0024245082
-
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
-
Chamberlain, J. S., Gibbs, R. A., Rainer, J. E., Nguyen, P. N. & Caskey, C. T. (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
Rainer, J.E.3
Nguyen, P.N.4
Caskey, C.T.5
-
7
-
-
0029998061
-
Geographic variation in human mtDNA control region sequence: The population history of Turkey and its relationship to European populations
-
Comas, D., Calafell, F., Mateu, E., Perez-Lezaun, A. & Bertranpetit, J. (1996). Geographic variation in human mtDNA control region sequence: The population history of Turkey and its relationship to European populations. Mol. Biol. Evol. 13, 1067-1077.
-
(1996)
Mol. Biol. Evol.
, vol.13
, pp. 1067-1077
-
-
Comas, D.1
Calafell, F.2
Mateu, E.3
Perez-Lezaun, A.4
Bertranpetit, J.5
-
8
-
-
0030895054
-
Mitochondrial DNA variation and the origin of the Europeans
-
Comas, D., Calafell, F., Mateu, E., Perez-Lezaun, A. & Bertraupetit, J. (1997). Mitochondrial DNA variation and the origin of the Europeans. Hum. Genet. 99, 443-449.
-
(1997)
Hum. Genet.
, vol.99
, pp. 443-449
-
-
Comas, D.1
Calafell, F.2
Mateu, E.3
Perez-Lezaun, A.4
Bertraupetit, J.5
-
9
-
-
0025354110
-
Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes
-
Cooke, A., Lanyon, W. G., Wilcox, D. E., Dornan, E. S., Kataki, A., Gillard, E. F., McWhinnie, A. J. M., Morris, A., Ferguson-Smith, M. A. & Connor, J. M. (1990). Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes. J. Med. Genet. 27, 292-297.
-
(1990)
J. Med. Genet.
, vol.27
, pp. 292-297
-
-
Cooke, A.1
Lanyon, W.G.2
Wilcox, D.E.3
Dornan, E.S.4
Kataki, A.5
Gillard, E.F.6
McWhinnie, A.J.M.7
Morris, A.8
Ferguson-Smith, M.A.9
Connor, J.M.10
-
10
-
-
0025738298
-
Genotype-phenotypp correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene
-
Covone, A. E., Lerone, M. & Romeo, O. (1991). Genotype-phenotypp 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.2
Romeo, O.3
-
11
-
-
0027195244
-
Patterns of deletions of the dystrophin gene in different European populations
-
Danieli, G. A., Mioni, F., Muller, C. R., Vitiello, L., Mostacciuolo, M. L. & 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
-
12
-
-
0024815723
-
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis reveals 115 deletions and 13 duplications
-
Den Dunnen, J. T., Grootscholten, P. M., Bakker, E., Blonden, L. A. J., Ginjaar, H. B., Wapenaar, M. C., Passen, H. M. B. van, Broecknoven, C. van, Pearson, P. L. & van Ommen, G. J. B. (1989). Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis reveals 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
Ginjaar, H.B.5
Wapenaar, M.C.6
Van Passen, H.M.B.7
Van Broecknoven, C.8
Pearson, P.L.9
Van Ommen, G.J.B.10
-
13
-
-
0023957073
-
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
-
Forrest, S. M., Cross, G. S., Flint, T., Speer, A., Robson, R. I. H. & Davies, K. E. (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, R.I.H.5
Davies, K.E.6
-
14
-
-
0024742222
-
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies
-
Gilgenkrantz, H., Chelly, J., Lambert, M., Recan, D., Barbot, J. C., van Ommen, G. J. B. & Kaplan, J. K. (1989). Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies. Genomics 5, 574-580.
-
(1989)
Genomics
, vol.5
, pp. 574-580
-
-
Gilgenkrantz, H.1
Chelly, J.2
Lambert, M.3
Recan, D.4
Barbot, J.C.5
Van Ommen, G.J.B.6
Kaplan, J.K.7
-
15
-
-
0024447280
-
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy
-
Hodgson, S., Hart, K., Abbs, S., Meekmatt, J., Rodillo, E., Bobrow, M. & Dubowitz, V. (1989). Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. J. Med. Genet. 26, 683-693.
-
(1989)
J. Med. Genet.
, vol.26
, pp. 683-693
-
-
Hodgson, S.1
Hart, K.2
Abbs, S.3
Meekmatt, J.4
Rodillo, E.5
Bobrow, M.6
Dubowitz, V.7
-
16
-
-
0024466501
-
The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion
-
Koenig, M., Beggs, A. M., Mayer, M., Schepf, S., Heindrich, K., Bettecker, T. 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.M.2
Mayer, M.3
Schepf, S.4
Heindrich, K.5
Bettecker, T.6
-
17
-
-
0024598162
-
Molecular deletion patterns in Duchenne and Becker type muscular dystrophy
-
Liechti-Gallati, S., Koenig, M., Kunkel, L. M., Frey, D., Boltshauser, E., Scheider, V., Braga, S. & Moser, H. (1989). Molecular deletion patterns in Duchenne and Becker type muscular dystrophy. 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
Scheider, V.6
Braga, S.7
Moser, H.8
-
18
-
-
0024582198
-
Gene deletions in X-linked muscular dystrophy
-
Lindlöf, M., Kiuru. A., Kaariainen, H., Kalimo, H., Lang, H., Pihko, H., Rapola, J., Somer, H., Somer, M., Savontaus, M. L. & de La Chapelle, A. (1989). Gene deletions in X-linked muscular dystrophy. Am. J. Hum. Genet. 44, 496-503.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 496-503
-
-
Lindlöf, M.1
Kiuru, A.2
Kaariainen, H.3
Kalimo, H.4
Lang, H.5
Pihko, H.6
Rapola, J.7
Somer, H.8
Somer, M.9
Savontaus, M.L.10
De La Chapelle, A.11
-
19
-
-
0024830683
-
Molecular deletion patterns in Duchenne muscular dystrophy patients
-
Lucotte, G., David, F. & Levy, C. (1989). Molecular deletion patterns in Duchenne muscular dystrophy patients. Ann. Genet. 32, 214-219.
-
(1989)
Ann. Genet.
, vol.32
, pp. 214-219
-
-
Lucotte, G.1
David, F.2
Levy, C.3
-
20
-
-
0018080152
-
Synthetic maps of human gene frequencies in Europeans
-
Menozzi, P., Piazza, A. & Cavalli-Sforza, L. (1978). Synthetic maps of human gene frequencies in Europeans. Science 201, 786-792.
-
(1978)
Science
, vol.201
, pp. 786-792
-
-
Menozzi, P.1
Piazza, A.2
Cavalli-Sforza, L.3
-
21
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, M., Dykes, D. D. & Polensky, H. F. (1988). A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16, 1215.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, M.1
Dykes, D.D.2
Polensky, H.F.3
-
22
-
-
0029895378
-
Paleloithic and neolithic lineages in the European mitochondrial gene pool
-
Richards, M, Corte-Real, H., Forster, P., Macaulay, V., Wilkinson-Herbots, H., Demaine, A., Papiha, S., Hedges, R., Bandelt, H.-J. & Sykes, B. (1996). Paleloithic and neolithic lineages in the European mitochondrial gene pool. Am. J. Hum. Genet. 59, 185-203.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 185-203
-
-
Richards, M.1
Corte-Real, H.2
Forster, P.3
Macaulay, V.4
Wilkinson-Herbots, H.5
Demaine, A.6
Papiha, S.7
Hedges, R.8
Bandelt, H.-J.9
Sykes, B.10
-
23
-
-
0027232968
-
Exon structure of the human dystrophin gene
-
Roberts, R. G., Coffey, A. J., Bobrow, M. & Bentley, D. R. (1993). Exon structure of the human dystrophin gene. Genomics 16, 536-538.
-
(1993)
Genomics
, vol.16
, pp. 536-538
-
-
Roberts, R.G.1
Coffey, A.J.2
Bobrow, M.3
Bentley, D.R.4
-
24
-
-
0031034656
-
Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients
-
Singh, V., Sinha, S., Mishra, S., Chaturvedi, L. S., Pradhan, S., Mittal, R. D. & Mittal. B. (1997). Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients. Hum. Genet. 99, 206-208.
-
(1997)
Hum. Genet.
, vol.99
, pp. 206-208
-
-
Singh, V.1
Sinha, S.2
Mishra, S.3
Chaturvedi, L.S.4
Pradhan, S.5
Mittal, R.D.6
Mittal, B.7
-
25
-
-
0025924487
-
Genetic evidence for the spread of agriculture in Europe by demie diffusion
-
Sokal, R. R., Oden, N. L. & Wilson, C. (1996). Genetic evidence for the spread of agriculture in Europe by demie diffusion. Nature 351, 143-145.
-
(1996)
Nature
, vol.351
, pp. 143-145
-
-
Sokal, R.R.1
Oden, N.L.2
Wilson, C.3
-
26
-
-
0025374776
-
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA
-
Upadhyaya, M., Smith, R. A., Thomas, N. S. T., Norman, A. M. & Harper, P. S. (1990). Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA. Clin. Genet. 29, 456-462.
-
(1990)
Clin. Genet.
, vol.29
, pp. 456-462
-
-
Upadhyaya, M.1
Smith, R.A.2
Thomas, N.S.T.3
Norman, A.M.4
Harper, P.S.5
-
27
-
-
0026535359
-
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients
-
Vitiello, L., Mostacciuolo, M. L., Oliviero, S., Schiavon, F., Nicoletti, L., Angelini, C. & Danieli, G. A. (1992). Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients. J. Med. Genet. 29, 127-130.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 127-130
-
-
Vitiello, L.1
Mostacciuolo, M.L.2
Oliviero, S.3
Schiavon, F.4
Nicoletti, L.5
Angelini, C.6
Danieli, G.A.7
|