-
1
-
-
0028214722
-
Towards high resolution maps of the mouse and human genomes - A facility for ordering markers to 0.1 cM resolution
-
1. Breen, M., Deakin, L., MacDonald, B., Miller, S., Sibson, R., Tarttelin, E., Avner, P., et al. (1994). Towards high resolution maps of the mouse and human genomes - A facility for ordering markers to 0.1 cM resolution. Hum. Mol. Genet. 3: 621-627.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 621-627
-
-
Breen, M.1
Deakin, L.2
MacDonald, B.3
Miller, S.4
Sibson, R.5
Tarttelin, E.6
Avner, P.7
-
2
-
-
0029166490
-
The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13
-
2. Brunialti, A. L., Poirier, C., Schmalbruch, H., and Guénet, J. L. (1995). The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13. Genomics 29: 131-135.
-
(1995)
Genomics
, vol.29
, pp. 131-135
-
-
Brunialti, A.L.1
Poirier, C.2
Schmalbruch, H.3
Guénet, J.L.4
-
3
-
-
0025260440
-
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-q13.3
-
3. Brzustowicz, L. M., Lehner, T., Castilla, L. H., Penchaszadeh, G. K., Wilhelmsen, K. C., Daniels, R. J., Davies, K. E., et al. (1990). Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-q13.3. Nature 344: 540-541.
-
(1990)
Nature
, vol.344
, pp. 540-541
-
-
Brzustowicz, L.M.1
Lehner, T.2
Castilla, L.H.3
Penchaszadeh, G.K.4
Wilhelmsen, K.C.5
Daniels, R.J.6
Davies, K.E.7
-
4
-
-
0028842926
-
A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients
-
4. Bussaglia, E., Clermont, O., Tizzano, E., Lefebvre, S., Bürglen, L., Cruaud, C., Urtizberea, J. A., et al. (1995). A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients. Nature Genet. 11: 335-337.
-
(1995)
Nature Genet.
, vol.11
, pp. 335-337
-
-
Bussaglia, E.1
Clermont, O.2
Tizzano, E.3
Lefebvre, S.4
Bürglen, L.5
Cruaud, C.6
Urtizberea, J.A.7
-
5
-
-
0028863567
-
Molecular analysis of spinal muscular atrophy in Chinese
-
5. Chang, J. G., Jong, Y. J., Huang, J. M., Wang, W. S., Yang, T. Y., Chang, C. P., Chen, Y. J., and Lin, S. P. (1995). Molecular analysis of spinal muscular atrophy in Chinese. Am. J. Hum. Genet. 57: 1503-1505.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1503-1505
-
-
Chang, J.G.1
Jong, Y.J.2
Huang, J.M.3
Wang, W.S.4
Yang, T.Y.5
Chang, C.P.6
Chen, Y.J.7
Lin, S.P.8
-
6
-
-
0029147787
-
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients
-
6. Gennarelli, M., Lucarelli, M., Capon, F., Pizzuti, A., Merlini, L., Angelini, C., Novelli, G., and Dallapiccola, B. (1995). Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients. Biochem. Biophys. Res. Commun. 213: 342-348.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.213
, pp. 342-348
-
-
Gennarelli, M.1
Lucarelli, M.2
Capon, F.3
Pizzuti, A.4
Merlini, L.5
Angelini, C.6
Novelli, G.7
Dallapiccola, B.8
-
7
-
-
0025330316
-
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy
-
7. Gilliam, T. C., Brzustowicz, L. M., Castilla, L. H., Lehner, T., Penchaszadeh, G. K., Daniels, R. J., Byth, B. C., et al (1990). Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Nature 345: 823-825.
-
(1990)
Nature
, vol.345
, pp. 823-825
-
-
Gilliam, T.C.1
Brzustowicz, L.M.2
Castilla, L.H.3
Lehner, T.4
Penchaszadeh, G.K.5
Daniels, R.J.6
Byth, B.C.7
-
9
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
9. Lefebvre, S., Burglen, L., Reboullet, S., Clermont, O., Burlet, P., Viollet, L., Benichou, B., et al. (1995). Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80: 155-165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
-
10
-
-
0025319713
-
Gene for proximal spinal muscular atrophies maps to chromosome 5q
-
10. Melki, J., Abdelhak, S., Sheth, P., Bachelot, M. F., Burlet, P., Marcadet, A., Aicardi, J., et al. (1990). Gene for proximal spinal muscular atrophies maps to chromosome 5q. Nature 344: 767-768.
-
(1990)
Nature
, vol.344
, pp. 767-768
-
-
Melki, J.1
Abdelhak, S.2
Sheth, P.3
Bachelot, M.F.4
Burlet, P.5
Marcadet, A.6
Aicardi, J.7
-
11
-
-
0025299356
-
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14
-
11. Melki, J., Sheth, P., Abdelhak, S., Burlet, P., Bachelot, M. F., Lathrop, M., Frézal, J., Munnich, A., and the French Spinal Muscular Atrophy investigators. (1990). Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. Lancet 336: 271-273.
-
(1990)
Lancet
, vol.336
, pp. 271-273
-
-
Melki, J.1
Sheth, P.2
Abdelhak, S.3
Burlet, P.4
Bachelot, M.F.5
Lathrop, M.6
Frézal, J.7
Munnich, A.8
-
12
-
-
0028200804
-
De novo and inherited deletions of the 5q13 region in spinal muscular atrophies
-
12. Melki, J., Lefebvre, S., Bürglen, L., Burlet, P., Clermont, O., Millasseau, P., Reboullet, S., et al. (1994). De novo and inherited deletions of the 5q13 region in spinal muscular atrophies. Science 264: 1474-1477.
-
(1994)
Science
, vol.264
, pp. 1474-1477
-
-
Melki, J.1
Lefebvre, S.2
Bürglen, L.3
Burlet, P.4
Clermont, O.5
Millasseau, P.6
Reboullet, S.7
-
13
-
-
0025668301
-
Gene-Link: A computer program in Pascal for backcross genetic linkage analysis
-
13. Montagutelli, X. (1990). Gene-Link: A computer program in Pascal for backcross genetic linkage analysis. J. Hered. 81: 490-491.
-
(1990)
J. Hered.
, vol.81
, pp. 490-491
-
-
Montagutelli, X.1
-
14
-
-
44949282843
-
Workshop report: International SMA collaboration
-
14. Munsat, T. L. (1991). Workshop report: International SMA collaboration. Neuromuscular Dis. 1: 81.
-
(1991)
Neuromuscular Dis.
, vol.1
, pp. 81
-
-
Munsat, T.L.1
-
15
-
-
0024309164
-
Animals models of amyotrophic lateral sclerosis and the spinal muscular atrophies
-
15. Paes, S., and de Jong, J. M. B. V. (1989). Animals models of amyotrophic lateral sclerosis and the spinal muscular atrophies. J. Neurol. Sci. 91: 231-258.
-
(1989)
J. Neurol. Sci.
, vol.91
, pp. 231-258
-
-
Paes, S.1
De Jong, J.M.B.V.2
-
16
-
-
0028905919
-
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
-
16. Rodrigues, N. R., Owen, N., Talbot, K., Ignatius, J., Dubowitz, V., and Davies, K. E. (1995). Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. Hum. Mol. Genet. 4: 631-634.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 631-634
-
-
Rodrigues, N.R.1
Owen, N.2
Talbot, K.3
Ignatius, J.4
Dubowitz, V.5
Davies, K.E.6
-
17
-
-
0025777705
-
A new mouse mutant with progressive motor neuronopathy
-
17. Schmalbruch, H. M. D., Jensen, H., Bjearg, M., Kamienniecka, Z., and Kurland, B. S. (1991). A new mouse mutant with progressive motor neuronopathy. J. Neuropathol. Exp. Neurol. 50: 192-204.
-
(1991)
J. Neuropathol. Exp. Neurol.
, vol.50
, pp. 192-204
-
-
Schmalbruch, H.M.D.1
Jensen, H.2
Bjearg, M.3
Kamienniecka, Z.4
Kurland, B.S.5
-
18
-
-
0028922174
-
PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy
-
18. Van der Steege, G., Grootscholten, P. M., Van der Vlies, P., Draaijers, T. G., Osingo, J., Cobben, J. M., Scheffer, H., and Buys, C. H. C. M. (1995). PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy. Lancet 345: 985-986.
-
(1995)
Lancet
, vol.345
, pp. 985-986
-
-
Van Der Steege, G.1
Grootscholten, P.M.2
Van Der Vlies, P.3
Draaijers, T.G.4
Osingo, J.5
Cobben, J.M.6
Scheffer, H.7
Buys, C.H.C.M.8
|