-
1
-
-
0026601924
-
Expansion of an Unstable DNA Region and Phenotypic Variation in Myotonie Dystrophy
-
Harley, H.G., Brook, J.D., Rundle, S., et al., Expansion of an Unstable DNA Region and Phenotypic Variation in Myotonie Dystrophy, Nature, 1992, vol. 355, pp. 545-546.
-
(1992)
Nature
, vol.355
, pp. 545-546
-
-
Harley, H.G.1
Brook, J.D.2
Rundle, S.3
-
2
-
-
0026584805
-
Detection of an Unstable Fragment of DNA Specific to Individuals with Myotonic Dystrophy
-
Buxton, J., Shelbourne, P., Davies, J., et al., Detection of an Unstable Fragment of DNA Specific to Individuals with Myotonic Dystrophy, Nature, 1992, vol. 355, pp. 547-548.
-
(1992)
Nature
, vol.355
, pp. 547-548
-
-
Buxton, J.1
Shelbourne, P.2
Davies, J.3
-
3
-
-
0026567370
-
Cloning of the Essential Myotonic Dystrophy Region and Mapping of the Putative Defect
-
Aslanidis, C., Jansen, G., Amemiya, C., et al., Cloning of the Essential Myotonic Dystrophy Region and Mapping of the Putative Defect, Nature, 1992, vol. 355, pp. 548-551.
-
(1992)
Nature
, vol.355
, pp. 548-551
-
-
Aslanidis, C.1
Jansen, G.2
Amemiya, C.3
-
4
-
-
0026566108
-
Molecular Basis of Myotonic Dystrophy: Expansion of a Trinucleotide (CTG) Repeat at 3′ End of a Transcript Encoding a Protein Kinase Family Member
-
Cambridge, Mass.
-
Brook, J.D., McCurrach, M.E., Harley, H.G., et al., Molecular Basis of Myotonic Dystrophy: Expansion of a Trinucleotide (CTG) Repeat at 3′ End of a Transcript Encoding a Protein Kinase Family Member, Cell (Cambridge, Mass.), 1992, vol. 68, pp. 799-808.
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
-
5
-
-
0027366978
-
Myotonic Dystrophy: Size and Sex-Dependent Dynamics of CTG Meiotic Instability, and Somatic Mosaicism
-
Lavedan, C., Hofmann-Radvanyi, H., Shelbourne, P., et al., Myotonic Dystrophy: Size and Sex-Dependent Dynamics of CTG Meiotic Instability, and Somatic Mosaicism, Am. J. Hum. Genet., 1993, vol. 52, pp. 875-883.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 875-883
-
-
Lavedan, C.1
Hofmann-Radvanyi, H.2
Shelbourne, P.3
-
6
-
-
0028156915
-
High Resolution Genetic Analysis Suggests One Ancestral Predisposing Haplotype for the Origin of the Myotonic Dystrophy Mutation
-
Novelle, C.E., Mahadevan, M.S., Barcelo, J.M., and Korneluk, R.G., High Resolution Genetic Analysis Suggests One Ancestral Predisposing Haplotype for the Origin of the Myotonic Dystrophy Mutation, Hum. Mol. Genet., 1994, vol. 3, pp. 45-51.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 45-51
-
-
Novelle, C.E.1
Mahadevan, M.S.2
Barcelo, J.M.3
Korneluk, R.G.4
-
7
-
-
0028794822
-
Normal Variation at the Myotonic Dystrophy Locus in Global Human Populations
-
Zerylnick, C., Torroni, A., Sherman, S., and Watten, S., Normal Variation at the Myotonic Dystrophy Locus in Global Human Populations, Am. J. Hum. Genet., 1995, vol. 56, pp. 123-130.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 123-130
-
-
Zerylnick, C.1
Torroni, A.2
Sherman, S.3
Watten, S.4
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