Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 132

2.

Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa.

Goldman A, Ramsay M, Jenkins T.

Ann Hum Genet. 1996 Jan;60(Pt 1):57-65.

PMID:
8835099
3.
4.

New founder haplotypes at the myotonic dystrophy locus in southern Africa.

Goldman A, Ramsay M, Jenkins T.

Am J Hum Genet. 1995 Jun;56(6):1373-8.

5.
6.

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.

Davies J, Yamagata H, Shelbourne P, Buxton J, Ogihara T, Nokelainen P, Nakagawa M, Williamson R, Johnson K, Miki T.

J Med Genet. 1992 Nov;29(11):766-9.

7.

Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.

Rubinsztein DC, Leggo J, Amos W, Barton DE, Ferguson-Smith MA.

Hum Mol Genet. 1994 Nov;3(11):2031-5.

PMID:
7874122
8.

CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand.

Theerasasawat S, Papsing C, Pulkes T.

J Clin Neurosci. 2010 Dec;17(12):1520-2. doi: 10.1016/j.jocn.2010.03.047. Epub 2010 Aug 30.

PMID:
20801043
9.

Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.

Ashizawa T, Monckton DG, Vaishnav S, Patel BJ, Voskova A, Caskey CT.

Genomics. 1996 Aug 15;36(1):47-53.

PMID:
8812415
10.

CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia.

Gennarelli M, Pavoni M, Cruciani F, De Stefano G, Dallapiccola B, Novelli G.

Hum Genet. 1999 Jul-Aug;105(1-2):165-7.

PMID:
10480373
11.

De novo myotonic dystrophy mutation in a Nigerian kindred.

Krahe R, Eckhart M, Ogunniyi AO, Osuntokun BO, Siciliano MJ, Ashizawa T.

Am J Hum Genet. 1995 May;56(5):1067-74.

12.

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K, et al.

Science. 1992 Mar 6;255(5049):1253-5.

PMID:
1546325
13.

A molecular protocol for diagnosing myotonic dystrophy.

Guida M, Marger RS, Papp AC, Snyder PJ, Sedra MS, Kissel JT, Mendell JR, Prior TW.

Clin Chem. 1995 Jan;41(1):69-72.

14.
15.

Myotonic dystrophy CTG repeats in an Italian population sample: evaluation of the polymorphism for forensic applications.

D'Apote L, Pelotti S, Bini C, Rimondi S, Ceccardi S, Ferri G, Pappalardo G.

Am J Forensic Med Pathol. 2000 Mar;21(1):86-9.

PMID:
10739235
16.

[Population analysis CTG trinucleotide repeats in the myotonin-protein kinase I gene].

Ivashchenko TE, Glazkov PB, Khromov-Borisov NN, Baranov VS.

Genetika. 1997 Sep;33(9):1287-90. Russian.

PMID:
9445821
17.

Somatic instability of CTG repeat in myotonic dystrophy.

Ashizawa T, Dubel JR, Harati Y.

Neurology. 1993 Dec;43(12):2674-8.

PMID:
8255475
18.

Variation of CTG-repeat number of the DMPK gene in muscle tissue.

Ansved T, Edström L, Grandell U, Hedberg B, Anvret M.

Neuromuscul Disord. 1997 May;7(3):152-5.

PMID:
9185177
19.

Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR.

Cheng S, Barceló JM, Korneluk RG.

Hum Mutat. 1996;7(4):304-10.

PMID:
8723679
20.

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Jansen G, Willems P, Coerwinkel M, Nillesen W, Smeets H, Vits L, Höweler C, Brunner H, Wieringa B.

Am J Hum Genet. 1994 Apr;54(4):575-85.

Supplemental Content

Support Center