-
1
-
-
49649108595
-
Mental retardation and lifetime events of Duchenne muscular dystrophy in Japan
-
Mochizuki H, Miyatake S, Suzuki M, et al,. Mental retardation and lifetime events of Duchenne muscular dystrophy in Japan. Intern. Med. 2008; 47: 1207-10.
-
(2008)
Intern. Med.
, vol.47
, pp. 1207-1210
-
-
Mochizuki, H.1
Miyatake, S.2
Suzuki, M.3
-
2
-
-
0034068415
-
Brain dystrophin, neurogenetics and mental retardation
-
DOI 10.1016/S0165-0173(99)00090-9, PII S0165017399000909
-
Mehler MF,. Brain dystrophin, neurogenetics and mental retardation. Brain Res. Brain Res. Rev. 2000; 32: 277-307. (Pubitemid 30177334)
-
(2000)
Brain Research Reviews
, vol.32
, Issue.1
, pp. 277-307
-
-
Mehler, M.F.1
-
3
-
-
0029894279
-
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency
-
DOI 10.1016/0960-8966(96)00016-8
-
Villanova M, Malandrini A, Biancotti R, et al,. Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency. Neuromuscul Disord. 1996; 6: 167-72. (Pubitemid 26171258)
-
(1996)
Neuromuscular Disorders
, vol.6
, Issue.3
, pp. 167-172
-
-
Villanova, M.1
Malandrini, A.2
Biancotti, R.3
Lofgren, A.4
Mongini, T.5
Six, J.6
Salvestroni, R.7
Parrotta, E.8
Van Broeckhoven, C.9
Paolozzi, C.10
Guazzi, G.11
-
4
-
-
0035202990
-
Central nervous system involvements in Duchenne/Becker muscular dystrophy
-
Kumagai T, Miura K, Ohki T, et al,. [Central nervous system involvements in Duchenne/Becker muscular dystrophy]. No To Hattatsu 2001; 33: 480-6. (Pubitemid 33115609)
-
(2001)
No To Hattatsu
, vol.33
, Issue.6
, pp. 480-486
-
-
Kumagai, T.1
Miura, K.2
Ohki, T.3
Matsumoto, A.4
Miyazaki, S.5
Nakamura, M.6
Ochi, N.7
Takahashi, O.8
-
5
-
-
27644468421
-
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies
-
DOI 10.1159/000087531
-
Bhat SS, Schmidt KR, Ladd S, et al,. Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies. Cytogenet. Genome Res. 2006; 112: 170-5. (Pubitemid 41579473)
-
(2006)
Cytogenetic and Genome Research
, vol.112
, Issue.1-2
, pp. 170-175
-
-
Bhat, S.S.1
Schmidt, K.R.2
Ladd, S.3
Kim, K.C.4
Schwartz, C.E.5
Simensen, R.J.6
DuPont, B.R.7
Stevenson, R.E.8
Srivastava, A.K.9
-
6
-
-
18544382489
-
The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation
-
DOI 10.1086/342208
-
Saito-Ohara F, Fukuda Y, Ito M, et al,. The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation. Am. J. Hum. Genet. 2002; 71: 637-45. (Pubitemid 34970135)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.3
, pp. 637-645
-
-
Saito-Ohara, F.1
Fukuda, Y.2
Ito, M.3
Agarwala, K.L.4
Hayashi, M.5
Matsuo, M.6
Imoto, I.7
Yamakawa, K.8
Nakamura, Y.9
Inazawa, J.10
-
7
-
-
0035577350
-
A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?
-
DOI 10.1016/S0168-9525(01)02446-5, PII S0168952501024465
-
Zechner U, Wilda M, Kehrer-Sawatzki H, Vogel W, Fundele R, Hameister H,. A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution? Trends. Genet. 2001; 17: 697-701. (Pubitemid 33097518)
-
(2001)
Trends in Genetics
, vol.17
, Issue.12
, pp. 697-701
-
-
Zechner, U.1
Wilda, M.2
Kehrer-Sawatzki, H.3
Vogel, W.4
Fundele, R.5
Hameister, H.6
-
8
-
-
34247570536
-
Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis
-
DOI 10.1007/s10038-007-0127-4
-
Hayashi S, Honda S, Minaguchi M, et al,. Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis. J. Hum. Genet. 2007; 52: 397-405. (Pubitemid 46669302)
-
(2007)
Journal of Human Genetics
, vol.52
, Issue.5
, pp. 397-405
-
-
Hayashi, S.1
Honda, S.2
Minaguchi, M.3
Makita, Y.4
Okamoto, N.5
Kosaki, R.6
Okuyama, T.7
Imoto, I.8
Mizutani, S.9
Inazawa, J.10
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