Similar articles for PMID: 7981744

Year	Number of Results
1990	1
1992	3
1993	11
1994	8
1995	2
1996	2
1997	1
1998	1
2000	1
2024	0

1

Brook JD. Brook JD. Nat Genet. 1993 Apr;3(4):279-81. doi: 10.1038/ng0493-279. Nat Genet. 1993. PMID: 7981744 No abstract available.

2

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.

Mahadevan MS, Foitzik MA, Surh LC, Korneluk RG. Mahadevan MS, et al. Genomics. 1993 Feb;15(2):446-8. doi: 10.1006/geno.1993.1087. Genomics. 1993. PMID: 8449517

3

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy.

Carango P, Noble JE, Marks HG, Funanage VL. Carango P, et al. Genomics. 1993 Nov;18(2):340-8. doi: 10.1006/geno.1993.1474. Genomics. 1993. PMID: 8288237

4

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Fu YH, Pizzuti A, Fenwick RG Jr, King J, Rajnarayan S, Dunne PW, Dubel J, Nasser GA, Ashizawa T, de Jong P, et al. Fu YH, et al. Science. 1992 Mar 6;255(5049):1256-8. doi: 10.1126/science.1546326. Science. 1992. PMID: 1546326

5

Brief report: reverse mutation in myotonic dystrophy.

Brunner HG, Jansen G, Nillesen W, Nelen MR, de Die CE, Höweler CJ, van Oost BA, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. N Engl J Med. 1993 Feb 18;328(7):476-80. doi: 10.1056/NEJM199302183280705. N Engl J Med. 1993. PMID: 8421477 Free article. No abstract available.

6

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG. Hunter AG, et al. Am J Med Genet. 1993 Feb 1;45(3):401-7. doi: 10.1002/ajmg.1320450330. Am J Med Genet. 1993. PMID: 8434633

7

Myotonic dystrophy with no trinucleotide repeat expansion.

Thornton CA, Griggs RC, Moxley RT 3rd. Thornton CA, et al. Ann Neurol. 1994 Mar;35(3):269-72. doi: 10.1002/ana.410350305. Ann Neurol. 1994. PMID: 8122879

8

A novel repeat structure at the myotonic dystrophy locus in a 37 repeat allele with unexpectedly high stability.

Leeflang EP, Arnheim N. Leeflang EP, et al. Hum Mol Genet. 1995 Jan;4(1):135-6. doi: 10.1093/hmg/4.1.135. Hum Mol Genet. 1995. PMID: 7711725 No abstract available.

9

[Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir].

Slominskiĭ PA, Popova SN, Fatkhlislamova RI, Akhmadeeva LR, Magzhanov RV, Khusnutdinova EK, Limborskaia SA. Slominskiĭ PA, et al. Genetika. 2000 Jun;36(6):844-8. Genetika. 2000. PMID: 10923268 Russian.

10

The usefulness of three biallelic restriction fragment length polymorphisms versus a polymorphic dinucleotide tandem repeat polymorphism at the low-density-lipoprotein receptor gene locus for diagnosis of familial hypercholesterolemia.

Weiss N, Gudnasson V, Ostwald P, Humphries S, Schuster H, Keller C. Weiss N, et al. Dis Markers. 1997 Nov;13(3):141-51. Dis Markers. 1997. PMID: 9405927

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