-
1
-
-
0023215347
-
X-linked dilated cardiomyopathy
-
BA Berko M Swift X-linked dilated cardiomyopathy N Engl J Med 316 1987 1186 1191
-
(1987)
N Engl J Med
, vol.316
, pp. 1186-1191
-
-
Berko, BA1
Swift, M2
-
3
-
-
0029824347
-
Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene
-
HJ Klamut LO Bosnoyan-Collins RG Worton PN Ray HL Davis Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene Hum Mol Genet 5 1996 1599 1606
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1599-1606
-
-
Klamut, HJ1
Bosnoyan-Collins, LO2
Worton, RG3
Ray, PN4
Davis, HL5
-
4
-
-
0030028518
-
A point mutation in the 5′ splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy
-
J Milasin F Muntoni GM Severini L Bartoloni M Vatta M Krajinovic A Mateddu A point mutation in the 5′ splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy Hum Mol Genet 5 1996 73 79
-
(1996)
Hum Mol Genet
, vol.5
, pp. 73-79
-
-
Milasin, J1
Muntoni, F2
Severini, GM3
Bartoloni, L4
Vatta, M5
Krajinovic, M6
Mateddu, A7
-
5
-
-
0027265702
-
Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy
-
F Muntoni M Cau A Ganau R Congiu G Arvedi A Mateddu MG Marrosu Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy N Engl J Med 329 1993 921 925
-
(1993)
N Engl J Med
, vol.329
, pp. 921-925
-
-
Muntoni, F1
Cau, M2
Ganau, A3
Congiu, R4
Arvedi, G5
Mateddu, A6
Marrosu, MG7
-
6
-
-
0028812128
-
Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy
-
F Muntoni MA Melis A Ganau V Dubowitz Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy Am J Hum Genet 56 1995 151 157
-
(1995)
Am J Hum Genet
, vol.56
, pp. 151-157
-
-
Muntoni, F1
Melis, MA2
Ganau, A3
Dubowitz, V4
-
8
-
-
0026321742
-
A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction
-
H Sakuraba K Ishii M Shimmoto H Yamada Y Suzuki A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction Brain Dev 13 1991 339 342
-
(1991)
Brain Dev
, vol.13
, pp. 339-342
-
-
Sakuraba, H1
Ishii, K2
Shimmoto, M3
Yamada, H4
Suzuki, Y5
-
9
-
-
0027193330
-
X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
JA Towbin JF Hejtmancik P Brink B Gelb XM Zhu JS Chamberlain ERB McCabe X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus Circulation 87 1993 1854 1865
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, JA1
Hejtmancik, JF2
Brink, P3
Gelb, B4
Zhu, XM5
Chamberlain, JS6
McCabe, ERB7
-
11
-
-
0027482335
-
Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy
-
K Yoshida S Ikeda A Nakamura M Kagoshima S Takeda S Shoji N Yanagisawa Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy Muscle Nerve 16 1993 1161 1166
-
(1993)
Muscle Nerve
, vol.16
, pp. 1161-1166
-
-
Yoshida, K1
Ikeda, S2
Nakamura, A3
Kagoshima, M4
Takeda, S5
Shoji, S6
Yanagisawa, N7
|