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Links from PubMed

Items: 11

1.

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

Friedrich U, Brunner H, Smeets D, Lambermon E, Ropers HH.

Hum Genet. 1987 Mar;75(3):291-3.

PMID:
2881880
2.

[Myotonic dystrophy of Steinert].

Junien C.

J Genet Hum. 1989 Jan;37(1):51-4. Review. French.

PMID:
2565953
3.

Myotonic dystrophy: update on progress to define the gene.

Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH, et al.

Aust Paediatr J. 1988;24 Suppl 1:66-9. Review.

PMID:
3060077
4.

Clinical and genetic heterogeneity in myotonic dystrophies.

Meola G.

Muscle Nerve. 2000 Dec;23(12):1789-99. Review.

PMID:
11102902
5.

Molecular analysis of human muscular dystrophies.

Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M.

Muscle Nerve. 1987 Mar-Apr;10(3):191-9. Review.

PMID:
2882417
6.

Advances in myotonic dystrophy: a clinical and genetic perspective.

Reardon W, Harper PS.

Curr Opin Neurol Neurosurg. 1992 Oct;5(5):605-9. Review.

PMID:
1392133
7.

[Current problems in myotonic dystrophy].

Weglewski A, JuryƄczyk J.

Neurol Neurochir Pol. 1998 Jul-Sep;32(4):903-11. Review. Polish.

PMID:
9864718
9.

Inheritance and pathogenicity of myotonic dystrophy.

Johnson K.

Mol Cell Biol Hum Dis Ser. 1993;3:85-110. Review. No abstract available.

PMID:
8111546
10.

Expanding complexity in myotonic dystrophy.

Groenen P, Wieringa B.

Bioessays. 1998 Nov;20(11):901-12. Review.

PMID:
9872056
11.

Report of the committee on the genetic constitution of chromosome 19.

Ropers HH, Pericak-Vance MA.

Cytogenet Cell Genet. 1990;55(1-4):218-28. Review. No abstract available.

PMID:
1981500

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