-
1
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
1. Bergoffen, J., Scherer, S. S., Wang, S., Oronzi Scott, M., Chance, P. F., and Fishbeck, K. H. (1993). Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science 262: 2039-2042.
-
(1993)
Science
, vol.262
, pp. 2039-2042
-
-
Bergoffen, J.1
Scherer, S.S.2
Wang, S.3
Oronzi Scott, M.4
Chance, P.F.5
Fishbeck, K.H.6
-
2
-
-
0020666103
-
Genetic deafness of central origin
-
2. Deol, M. S., Frank, M. P., Steel, K. P., and Bock, G. R. (1983). Genetic deafness of central origin. Brain Res. 258: 177-179.
-
(1983)
Brain Res.
, vol.258
, pp. 177-179
-
-
Deol, M.S.1
Frank, M.P.2
Steel, K.P.3
Bock, G.R.4
-
3
-
-
0026740023
-
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridisation
-
3. Fantes, J. A., Bickmore, W. A., Fletcher, J. M., Ballesta, F., Hanson, I., and van Heyningen, V. (1992). Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridisation. Am. J. Hum. Genet. 51: 1286-1294.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1286-1294
-
-
Fantes, J.A.1
Bickmore, W.A.2
Fletcher, J.M.3
Ballesta, F.4
Hanson, I.5
Van Heyningen, V.6
-
4
-
-
0020793569
-
A technique for radio-labelling DNA restriction endonuclease fragments to high specific activity
-
4. Feinberg, A. P., and Vogelstein, B. (1983). A technique for radio-labelling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132: 6-13.
-
(1983)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
5
-
-
0028204901
-
Periaxin, a novel protein of myelinating Schwann cells with a possible role in axonal ensheathment
-
5. Gillespie, C. S., Sherman, D. L., Blair, G. E., and Brophy, P. J. (1994). Periaxin, a novel protein of myelinating Schwann cells with a possible role in axonal ensheathment. Neuron 12: 479-508.
-
(1994)
Neuron
, vol.12
, pp. 479-508
-
-
Gillespie, C.S.1
Sherman, D.L.2
Blair, G.E.3
Brophy, P.J.4
-
6
-
-
0027221141
-
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin Po gene
-
6. Hayasaki, K., Himoro, M., Sato, W., Takada, G., Uyemura, K., Shimizu, N., Bird, T. D., Conneally, P. M., and Chance, P. F. (1993). Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin Po gene. Nature Genet. 5: 31-34.
-
(1993)
Nature Genet.
, vol.5
, pp. 31-34
-
-
Hayasaki, K.1
Himoro, M.2
Sato, W.3
Takada, G.4
Uyemura, K.5
Shimizu, N.6
Bird, T.D.7
Conneally, P.M.8
Chance, P.F.9
-
7
-
-
0003903343
-
-
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
-
7. Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989). "Molecular Cloning: A Laboratory Manual," Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
8
-
-
0029615322
-
Periaxin expression in myelinating schwann cells: Modulation by axon-glial interactions and polarized localization during development
-
8. Scherer, S. S., Xu, Y-T., Bannerman, P., Sherman, D. L., and Brophy, P. J. (1995). Periaxin expression in myelinating Schwann cells: Modulation by axon-glial interactions and polarized localization during development. Development 121: 4265-4273.
-
(1995)
Development
, vol.121
, pp. 4265-4273
-
-
Scherer, S.S.1
Xu, Y.-T.2
Bannerman, P.3
Sherman, D.L.4
Brophy, P.J.5
-
9
-
-
0029135193
-
The molecular basis of the neuropathies of mouse and human progress in brain research
-
9. Snipes, G. J., Suter, U., Welcher, A. A., and Shooter, E. M. (1995). The molecular basis of the neuropathies of mouse and human progress in brain research. Prog. Brain Res. 105: 319-325.
-
(1995)
Prog. Brain Res.
, vol.105
, pp. 319-325
-
-
Snipes, G.J.1
Suter, U.2
Welcher, A.A.3
Shooter, E.M.4
-
10
-
-
0000169676
-
Quivering, a new first chromosome mutation in mice
-
10. Yoon, C. H., and Lees, E. P. (1957). Quivering, a new first chromosome mutation in mice. J. Hered. 48: 176-180.
-
(1957)
J. Hered.
, vol.48
, pp. 176-180
-
-
Yoon, C.H.1
Lees, E.P.2
|